Click Sl.No. for the link to the particular paper
161
Direct Pyridoannulation of 2-Chloro-3-Carbonyl Indoles with 1,3-Dipolar Azomethine ylides: An Adaptable, One-Flask Access to Substituted β-Carboline-1-Carboxylates
Rahul Balu Dadhe, Srihari Pabbaraja,* Goverdhan Mehta*
J. Org. Chem. 2026, 0000 (https://doi.org/10.1021/acs.joc.5c02829)
160
Stereoselective Synthesis of C1–C18 Fragment with Macrocyclic Framework of Marine Cytotoxic (-)-Callyspongiolide
SankaraRao Patta, Naresh Gantasala, Pradeep P Desale and Srihari Pabbaraja*
Eur J. Org. Chem., 2026, 0000.
159
Continuous Flow Synthesis of α-Lipoic Acid Using Microreactors
Navya Manthani, Chandrasekhar Latchubugata, Srihari Pabbaraja, Sreepriya Vedantham*
SADH, 2026, 0000 (Accepted manuscript)
158
Comparative Assessment of a Novel Neuroprotectant against Citicoline in a Thrombus-Induced Cerebral Ischemia Mouse Model
Soumya Ghosh, Roli Kushwaha, Shashikant Patel, Oja Joachyutharayalu, Swikriti Paul, Srihari Pabbaraja, Sumana Chakravarthy, Arvind Meena
IJEB, 2026, 64, (06).
157
Stereoselective Synthesis of Protected 12-Membered Macrolide Antibiotic 13E-Disciformycin B Aglycone
Naresh Gantasala, Sankara Rao Patta, Srihari Pabbaraja*
Eur. J. Org. Chem. 2026, 29 (3), e202500950
Flow Process for Production of Crisaborole Using Organolithium Chemistry with Control over Impurity Formation
Chander Singh Bohara, Manjinder Singh Phull, Srihari Pabbaraja*
ACS Omega 2025, 10, 55920-55931.
Stitching ynones with indolin-2-thiones: An eco-friendly reaction cascade towards functionalized thiopyrano[2,3-b]indoles and their inceptive optoelectronic profiling.
Alagesan Balasubramani, Rupali Shivachalappa Salgar, Lingamallu Giribabu, Srihari Pabbaraja,* Goverdhan Mehta*
Org. Biomol. Chem. 2025, 23, 9100-9104.
Stereoselective Total Synthesis of Cytotoxic Cyclodepsipeptide Menominin B: Call for Revision of Proposed Structure
Siva Ramakrishna Paipuri,a,b Padyabharati Nayak,a,b Resmi Kattukaran Raman,c Sai Balaji Andugulapati,b,d Srihari Pabbaraja
Org. Biomol. Chem. 2025, 23, 7115-7119
https://doi.org/10.1039/D5OB01067E
Heavy Atom Integration in 2-Hydroxymethylquinoline: A Rational Strategy for Enhanced Two-Photon Absorption-Mediated Tumor and Nuclear-Targeted Drug Delivery in Triple-Negative Breast Cancer
Pragya Trivedi, Manotosh Pramanik, Venkatesh Sarampally, Pritam Das, Bhuvaneshwari Vuyyla, Debasish Swain, Srihari Pabbaraja, Bipul Pal, Avijit Jana*
J. Med. Chem. 2025, 68(13), 13836-13857
https://doi.org/10.1021/acs.jmedchem.5c00703
K. A. Sudarshana, Alagesan Balasubramani, Srihari Pabbaraja* and Goverdhan Mehta,* One-Flask, Telescoped Synthesis of Pyrano[3,2‑b]indol-2-ones from O‑Nitroynones and β‑Ketoesters: Further Advancement to Functionalized Carbazoles
J. Org. Chem. 2025, 90, 4397-4408
DOI:https://doi.org/10.1021/acs.joc.5c00266
Shweta Singh, Rahul Balu Dadhe, Srihari Pabbaraja*, Goverdhan Mehta*
Benzannulation of Functionally Enhanced Indole-3-carbaldehydes with Ynones and Alkynoates: A Domino Approach to Bioactive Carbazoles─Synthesis of Clauolenzole A, Calothrixin A & B, Methyl Carbazole-3-carboxylate, and Quinocarbazole
J. Org. Chem. 2025, 90, 6, 2510-2520
Manohar Surve, Naresh Gantasala, Sudheer Pudi, and Srihari Pabbaraja*
A linear approach for the total synthesis of sex pheromone (3S,5R,6S)-6-isopropyl-3,5-dimethyltetrahydro-2H-pyran-2-one and prelactone B
Synth. Commun. 2025, 55(4), 305–314.
Siva Ramakrishna Paipuri, Srihari Pabbaraja*
A classical peptide coupling approach for the total synthesis of simnotrelvir
Tetrahedron 2024, 168, 134342.
Joachyutharayalu Oja, Sanjeev Kumar and Srihari Pabbaraja*
Visible-light-mediated flow protocol for Achmatowicz rearrangement
Beilstein J. Org. Chem. 2024, 20, 2493–2499.
Chitrakshi Pant, Genji Sukumar, Vidya Jyothi Alli, Surender Singh Jadav,* Srihari Pabbaraja* and Shasi V Kalivendi*
Allosteric activation of SIRT1 by 2,4-dihydroxy-azaflavanone ameliorates MPP+ mediated dysfunction in mitochondrial biogenesis and bioenergetics: Implications for Parkinson’s disease
ACS Chemical Neuroscience, 2024, 15(15), 2870-2883.
Alagesan Balasubramani, K. A. Sudarshana, Roli Kushwaha, Sumana Chakravarty, Srihari Pabbaraja* and Goverdhan Mehta,*
One flask cascade approach to complex pyrano[2,3-c]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling
Chem. Commun. 2024, 60, 8443-8446
Neeraj Kumar Chouhan, Abhisheik Eedara, Mamta N Talati, Sudha S. S. S. S Ambadipudi, Sai Balaji Andugulapati,* Srihari Pabbaraja,*
Glucosyltriazole amphiphile treatment attenuates breast cancer by modulating the AMPK signaling
Drug Dev. Res. 2024, 85, e22215.
Saumitra Sengupta,* Srihari Pabbaraja,* Goverdhan Mehta*.
Natural products from the human microbiome: an emergent frontier in organic synthesis and drug discovery.
Org. Biomol. Chem. 2024, 22, 4006-4030
K. A. Sudarshana, Manas Jyoti Sarma, Mydhili Radhakrishnan, Sumana Chakravarty, Pabbaraja Srihari * and Goverdhan Mehta,* A protocol for directly accessing geminal C-4 diarylated pyrazol-5(4H)-ones via tandem C–H aryne insertion and their inceptive neurobiological evaluation.
Org. Biomol. Chem. 2024, 22, 714-719.
142
Rajesh Nasam, Srihari Pabbaraja*
A convergent approach for the synthesis of C14-C26 fragment of anti-cancer drug eribulin mesylate
Synthesis. 2024, 56, 462-468.
141
Mani Sharma, S.S.S.S. Sudha Ambadipudi, Neeraj Kumar Chouhan, V. Lakshma Nayak, Srihari Pabbaraja,* Sai Balaji Andugulapati,* Ramakrishna Sistla*
Design, synthesis and biological evaluation of novel cationic liposomes loaded with melphalan for the treatment of cancer
Bioorg. Med. Chem. Lett. 2023, 97, 129549.
Manas Jyoti Sarma, K A Sudarshana, Srihari Pabbaraja,* Goverdhan Mehta*
Diversified Stitching of Ynones with Oxindole-3-oxy acrylates: One-Flask Spiro-annulation Protocol towards Assorted 3H/5H-Spiro[furan-2,3'-indolin]-2'-ones, J. Org. Chem. 2023 88(16), 12131-12140.
Saumitra Sengupta,* Srihari Pabbaraja,* Goverdhan Mehta*.
C-H Modification of natural products: a minimalist enabling tactic for drug discovery, API processing and bioconjugation. Chem Commun. 2023, 59, 9445-9456.
Sandeep Vaidya, Annie Mohod, Abhisheik Chowday Eedara, Saibalaji Andugulapati*, Srihari Pabbaraja*,
Synthesis and characterization of novel cationic lipid: Efficient siRNA delivery and anticancer activity of survivin-siRNA lipoplexes for the treatment of lung and breast cancers. Chem Med Chem. 2023, 18 (16), e202300097
Gantasala, Naresh; Fournet, Corentin; Le Roch, Myriam; LALLI, Claudia; Pabbaraja, Srihari*; Gouault, Nicolas*,
Accessing Spiropiperidines as Original 3D-Fragments from Dihydropyridones through Tandem Triflation-Allylation and RCM, Org. Biomol. Chem. 2023, 21, 5245.
Deepak Kumar Jaiswal, Dnyaneshwar Aand, Puchakayala Krishna Rao, Sibaji Nandi, Srihari Pabbaraja, Ajay K Singh*,
Diazomethane Mediated Sealing of Carboxylic Moieties in MOFs: Opening Doors for Increased Hydrophobicity
Applied Surface Science, 2023, 620, 156788.
Manas Jyoti Sarma, K A Sudarshana, Srihari Pabbaraja* and Goverdhan Mehta*
An Approach to Functionally Embellished o-Alkynylbenzoates or Furan-3(2H)-ones from Diynones and DMAD: Controlled Divergence and Product Selectivity.
J. Org. Chem. 2023, 88, 6, 3945–3953
134
Bhushan Mahajan, Dnyaneshwar Aand, Mandeep Purwa, Taufiqueahmed Mujawar, Subhash Ghosh, Srihari Pabbaraja,* Ajay Kumar Singh*
Elements-continuous-flow platform for coupling reaction and Antiviral daclatasvir API synthesis,
Synthesis 2023, 55, A-K
Ruchi Chauhan, Abhilash Rana, Subhash Ghosh, P. Srihari, Ajay K Singh*
Micro-total process system machine (m-TPSM) for rapid synthesis of antiretroviral darunavir,
React. Chem. Eng. 2023, 8, 908-916.
Ravi Gurram, Srihari Pabbaraja*
A convergent approach for protected (+)-paecilomycin F,
Lett. Org. Chem. 2023, 20, 185-192.
Chandra Shekhar, Rajesh Nasam, Siva Ramakrishna Paipuri, Prakash Kumar, Kiranmai Nayani, Srihari Pabbaraja, Prathama S. Mainkar, Srivari Chandrasekhar*
Total synthesis of antiviral drug, nirmatrelvir (PF-07321332),
Tetrahedron Chem 2022, 4, 100033.
Bharath Kumar Yasam, Srihari Pabbaraja*
Total synthesis of marine-derived azole resistant antifungal agent (-)-melearoride A and antibiotic (-)-PF1163B
SynOpen, 2022, 6, 227-237, DOI: 10.1055/a-1942-6969
Saumitra Sengupta,* Srihari Pabbaraja,* Goverdhan Mehta* Domino reactions through recursive anionic cascades: The advantageous use of nitronates, Eur. J Org. Chem. 2022, 2022(42), e202200945
128
Ganesh Kumar Raut, Genji Sukumar, Moumita Chakrabarti, Jolly Janette Mendonza, Srihari Pabbaraja, B. Jagan Mohan Reddy, Ramakrishna Sistla, Sai Balaji Andugulapati, Manika Pal Bhadra*
Anticancer effect and apoptosis induction by azaflavanone derivative in human prostate cancer cells
Apoptosis, 2022, 1-15
Abhilash Rana, Bhanwar Kumar Malviya, Deepak Kumar Jaiswal, Srihari Pabbaraja, Ajay K Singh*
Solar tracker integrated microreactor for real-time sunlight induced ketene formation and API synthesis
Green Chemistry, 2022, 24, 4794-4799. https://pubs.rsc.org/en/Content/ArticleLanding/2022/GC/D2GC00649A
Rajesh Nasam, Srihari Pabbaraja*
A convergent total synthesis of resorcylic acid lactones zeaenol and cochliomycin A
Tetrahedron Lett. 2022, 97, 153777 https://doi.org/10.1016/j.tetlet.2022.153777
N. K. Chouhan, Sudarshana K. Ananthabhat, Sandeep Vaidya, P. Srihari*
A scalable process for the synthesis of key intermediates novoldiamine & hydroxynovaldiamine and their utility in chloroquine, hydroxychloroquine and mepacrine synthesis
Synthetic Commun. 2022, 52 (7), 1004-1011 https://doi.org/10.1080/00397911.2022.2061358.
Gandhari Kishor, Vankudoth Ramesh, Vadithya Ranga Rao, Srihari Pabbaraja* and Praveen Reddy Adiyala*
Regioselective C-3-alkylation of quinoxalin-2(1H)-ones via C–N bond cleavage of amine derived Katritzky salts enabled by continuous-flow photoredox catalysis
RSC Advances 2022, 12, 12235-12241.
Manas Jyoti Sarma, Sana Jindani, Bishwajit Ganguly, Srihari Pabbaraja* and Goverdhan Mehta*
Tandem Michael-antiMichael Addition Mediated Orthogonal Strapping of Diynones: Regioselective Spirocyclopentannulation of Oxindoles and Pyrazolones and DFT Validation
J. Org. Chem. 2022, 87, 1, 884-891.
Vinay Kumar Sthalam, Bhushan Mahajan, Purushotham Reddy Karra, Ajay K. Singh,* Srihari Pabbaraja*
Sulphonated Graphene Oxide Catalyzed Continuous Flow Pyrazolo Pyrimidinones, Sildenafil and other PDE-5 Inhibitors Synthesis
RSC Advances, 2021, 12, 326-330.
Chitrakshi Pant, Moumita Chakrabarti, Jolly Janette Mendonza, Ganganna Bogonda, Srihari Pabbaraja* and Manika Pal Bhadra*
Aza-flavanone diminishes Parkinsonism in Drosophila melanogaster parkin mutant
ACS Chemical Neuroscience, 2021, 12, 4380-4392.
Sanjeev Kumar, Bhushan Mahajan, Bhanwar Malviya, Genji Sukumar, Srihari Pabbaraja, Ajay Singh*
Electricity-induced micro-flow C-H/N-H alkyne annulation: A greener approach to access heteroaromatic compounds
React. Chem. & Eng. 2021, 6, 1801-1805
Shweta Singh, Sharanya Nerella, Srihari Pabbaraja*, Goverdhan Mehta*
Stitching Ynones with Nitromethanes: Domino Synthesis of Functionally Enriched Benzofurans and Benzothiophenes
J. Org. Chem., 2021, 86, 12093-12106
P. Srihari*, Y. Bharath Kumar, B. Suresh
Gram Scale Synthesis of Honokiol
Org. Prep. Proced. Int. 2021, 24, 0000-0000
Krishna A.; Basetty, S.; Nasam, R.; Salte, S.; Raji Reddy, Ch.; Sudhakar, G.; Srihari, P .; Chandrasekhar, S.; Prathama, S. M.; Kumaraguru, T.*; Subhash, G*
Chemo-enzymatic process for the preparation of (S)-7-((tert-butyldiphenylsilyl)oxy)hept-1-yn-4-ol in a continuous packed-bed reactor (PBR), a key intermediate for eribulin synthesis
Org. Process Res. Dev. 2020 , 24( 11), 2657-2664
Abhilash Rana, Bhusha Mahajan, Subhash Ghosh, Srihari Pabbaraja* and Ajay K Singh*
Integrated Multi-Step Continuous Flow Synthesis of Daclatasvir Without Intermediate Purification and Solvent Exchange
React. Chem. Eng. 2020 , 5, 2109-2114
Nagarjuna Chary Ragi , Ganga Reddy Velma , Pavan Kumar Pallerla , Sana Siddiqua , Veeresham Alugonda , Hari Krishna Reddy Rachamalla , Srihari Pabbaraja , Prabhakar Sripadi*
Identification and characterization of forced degradation products of vortioxetine by LC/MS/MS and NMR
Journal of Pharmaceutical and Biomedical Analysis, 2020 , 188, 113442
Shweta Singh, Sharanya Nerella, Srihari Pabbaraja ,* Goverdhan Mehta*
Access to 2-Alkyl/Aryl-4-(1H)-Quinolones via Orthogonal NH 3 Insertion into o-Haloaryl Ynones: Total Synthesis of Bioactive Pseudanes Graveoline, Graveolinine, and Waltherione F
Org. Lett. 2020, 22, 1575-1579
Kumar, Sanjeev, Aand Dnyaneshwar, Pabbaraja Srihari, Kim Dong Pyo, Singh Ajay K*
An Integrated Microfluidic Photo-Flow ( μ -PFP) for Direct Upconversion of Exhaust Gas to Value-Added Chemicals
ACS Sustainable Chem. Eng. 2019 , 7 (24), 19605-19611
Jurupula Ramprasad, Vinay Kumar Sthalam, Rama Linga Murthy Thampunuri, Supriya Bhukya, Ramesh Ummanni, Sridhar Balasubramanian, Srihari Pabbaraja *
Synthesis oand evaluation of a novel quinoline-triazole analogs for anti tubercular properties via molecular hybridisation approach
Bioorg. Med. Chem. Lett. 2019 , 29 , 126671
Bhushan Mahajan, Taufiqueahmed Mujawar, Subhash Ghosh, Srihari Pabbaraja,* Ajay K Singh*
Micro-Electro-Flow Reactor (micro-EFR) System for Ultra-Fast Arene Synthesis, and Manufacturing of Daclatasvir
Chem. Commun. 2019 , 55, 11852-11855
Velma Ganga Reddy, T. Srinivasa Reddy,* Chetna Jadala, M. Soumya Reddy, Faria Sultana, Ravikumar Akunuri, Suresh K. Bhargava, Donald Wlodkowic, P. Srihari* , Ahmed Kamal*
Pyrazolo-benzothiazole hybrids: Synthesis, anticancer properties and evaluation of antiangiogenic activity using in vitro VEGFR-2 kinase and in vivo transgenic zebrafish model
Eur. J. Med. Chem. 2019 , 182, 111609
S. Vinay Kumar, Ajay K Singh*, Srihari Pabbaraja *
An Integrated Continuous Flow Micro-Total Ultra-Fast Process System (μ-TUFPS) for the Synthesis of Celecoxib and other Cyclooxygenase Inhibitors
Org. Process Res. Dev. 2019, 9, 1892-1899
Shweta Singh, Ramesh Samineni, Srihari Pabbaraja *, Goverdhan Mehta *
Benzannulation of Arynes with Dimethylacetonedicarboxylates via an Insertion-Fragmentation-Dieckman Aromatization Cascade: Expeditious Entry to Naphthoresorcinols and Binaphthoresorcinols
Tetrahedron 2019 , 75 , 2923-2932
Shweta Singh, Ramesh Samineni, Srihari Pabbaraja *, Goverdhan Mehta *
A General Carbazole Synthesis via Stitching of Indole-Ynones with Nitromethanes: Application to Total Synthesis of Carbazomycin A, Calothrixin B and Staurosporinone
Organic Lett. 2019 , 21 , 3372-3376
Dnyaneshwar Aand, Bhushan Mahajan, Srihari Pabbaraja *, Ajay K Singh*
Integrated Continuous Flow/Batch Protocol for the Photoreduction of ortho-Methyl Phenyl Ketones using Water as Hydrogen Source
Reaction Chemistry & Engineering , 2019 , 4 , 812-817
Shweta Singh, Ramesh Samineni, Srihari Pabbaraja *, Goverdhan Mehta *
Nitromethane as a Recursive Carbanion Source for Domino Benzoannulation with Ynones: One-pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine
Angew. Chem. Int. Ed.2018 , 57 , 16847, Angew. Chem. 10.1002/ange.201810652
Pa marthi Gangadhar, Sayini Ramakrishna, Ponneri Venkateswarlu,Pabbaraja Srihari *
Stereoselective Total Synthesis and Structural Revision of Diacetylenic Diol Natural Products Strongylodiols H and I
Beilstein J. Org. Chem. 2018 , 14,2313-2320
Srihari Pabbaraja ,* Naresh Gantasala, Sridhar Ydhyam , Hari Krishna Namballa, Subhashini Gundeboina, Mallikharjuna R. Lambu, Sanjeev Meena, Dipak Datta
Synthesis and biological evaluation of 12-, 13-, 14-membered macrolides and open chain 2,6- trans -disubstituted dihydropyran analogues for aspergillides
Tetrahedron Lett. 2018, 59 , 2570-2576
P abbaraja Srihari ,* Naresh Gantasala, Suresh Borra
Stereoselective total synthesis of non-contiguous polyketide natural product (-)-dolabriferol
Eur. J. Org. Chem.2018, 1230-1240
V. Ganga Reddy, Srinivasa Reddy Bonam, T. Srinivasa Reddy*, Ravikumar Akunuri, V.G.M. Naidu, V. Lakshma Nayak, Suresh K. Bhargava, H.M. Sampath Kumar, P. Srihari* , Ahmed Kamal*
4- beta-amidotriazole linked podophyllotoxin congeners: DNA topoisomerase-IIa inhibition and potential anticancer agents for prostate cancer
Eur J Med. Chem. 2018, 144, 595-611
Ramesh Samineni, Jaipal Madapa, Srihari Pabbaraja ,* Goverdhan Mehta*
Stitching Oxindoles and Ynones in a Domino Process:Access to Spirooxindoles and Application to a Short Synthesis of Spindomycin B
Org. Lett. 2017, 19, 6152-6155
Ramakrishna S, Srihari P .*
Studies on the total synthesis of antibiotic macrolactin S; A conventional approach for the synthesis of C1-C9 and C10-C24 fragments
Synthesis, 2017, 50, 663-675
Ramesh Samineni, Jaipal Madapa, Pabbaraja Srihari ,* Goverdhan Mehta*
Spiroannulation of Oxindoles via Aryne and Alkyne Incorporation: Substituent-Diverted, Transition-Metal-Free, One-Pot Access to Spirooxindoles
Org. Lett. 2017, 19, 3119-3122
Bogonda Ganganna, Pabbaraja Srihari , Jhillu Singh Yadav*
Studies towards the total synthesis of cruentaren A and B: Stereoselective synthesis of fragments C1-C11, C12-C22 and C23-C28
Tetrahedron Lett.2017, 58, 2685-2689
Pamarthi Gangadhar, Pallavagary Rajesh, Srihari Pabbaraja *
Stereoselective Total Syntheses of (R)-Strongylodiols A, B, C and D
ChemistrySelect, 2017, 2, 4106-4110
Pranav Chintamani Joshi, Ramesh Samineni, Dwaipayan Bhattacharya, Bommana Raghunath Reddy, Lenin Veeraval, Tapatee Das, Swati Maitra, Abhipradnya Bipin Wahul, Shailaja Karri, Srihari Pabbaraja , Goverdhan Mehta, Arvind Kumar, Sumana Chakravarty*
A 2-oxa-spiro[5.4]decane scaffold displays neurotrophic, neurogenic and anti-neurotrophic, neurogenic and anti-neuroinflammatory activities with high potential for development as a versatile CNS therapeutic
Scientific Reports, 2017, Art no.1492
Jhillu S. Yadav,* Sravanth Kumar Amrutapu, and Srihari Pabbaraja *
Studies Towards the Synthesis of Stereoisomer of Acremolide B
ChemistrySelect, 2017, 2, 1850-1853
A. Sravanth Kumar, P. Srihari ,* J. S.Yadav,* Ahmad, A. Alghamdi
Stereoselective total synthesis of stigmolone: The fruiting body inducing pheromone
Synthesis 2017 , 49, 1702-1706
92
A. Sravanth Kumar, K. Praneeth, P. Srihari,* J. S. Yadav*
First stereoselective total synthesis and reconfirmation of absolute structure of nonenolide (-)-stagonolide D
Tetrahedron Lett. 2016 , 58, 509-511
91
Ramesh Samineni, Chandramohan Reddy C. Bandi,Pabbaraja Srihari* and Goverdhan Mehta*
Multiple Aryne Insertions into Oxindoles: Synthesis of Bioactive 3,3-Diarylated Oxindoles and Dibenzo[b,e]azepin-6-ones
Org. Lett . 2016 , 18, 6184–6187
P. Sankara Rao and P. Srihari*
A facile approach for the synthesis of C13-C24 fragment of maltepolides A, C and D
Org. & Biomol. Chem. 2016, 14, 9629-9638
B. Suresh, A. Sravanth Kumar, P. Srihari ,* J. S. Yadav*
Stereoselective total synthesis of palmyrolide A via intramolecular trans N-methyl enamide formation
Tetrahedron Lett.2016 , 57 , 4456-4459
Pamarthi Gangadhar, A. Sathish Reddy, Pabbaraja Srihari*
A facile approach for the total synthesis of neurotrophic diyne tetraol petrosiol A and petrosiol E
Tetrahedron 2016, 72, 5807-5817
Ramesh Samineni, Pabbaraja Srihari* , Goverdhan Mehta*
Versatile Route to Benzoannulated Medium-Ring Carbocycles via Aryne Insertion into Cyclic 1,3-Diketones: Application to a Synthesis of Radermachol
Org. Lett. 2016, 18 , 2832-2835
J. S. Yadav*, B. Suresh and P. Srihari *
Expedient synthesis of large-ring trans-enamide macrolides through CuI mediated intramolecular coupling of vinyl iodide with amide; Total synthesis of palmyrolide A
Eur. J. Org. Chem. 2016, 2509-2513
B . Mahankali, P. Srihari*
Total synthesis of antiplasmodial resorcylic acid lactone paecilomycin F
ARKIVOC 2016, 123-136
Sumana Chakravarty,* Swati Maitra, R Gajendra Reddy, Tapatee Das, Priya Jhelum, Scherazad Kootar, Wenson D Rajan, Anumita Samanta, Ramesh Samineni,
Srihari Pabbaraja , Steven G Kernie, Goverdhan Mehta & Arvind Kumar
A novel natural product inspired scaffold with robust neurotrophic, neurogenic and neuroprotective action
Scientific Reports, 2015 , Art no.14134
J. S. Yadav,* B. Suresh, P. Srihari *
Stereoselective total synthesis of marine macrolide sanctolide A
Eur. J. Org. Chem.2015 , 5856-5863
B. Mahankali, P. Srihari *
A carbohydrate approach for the first total synthesis of cochliomycin C. Stereoselective total synthesis of paecilomycin E, paecilomycin F and 6’-epi-cochliomycin C
Eur. J. Org. Chem.2015 , 3983-3993
Wasim Ahmed, Prathama S. Mainkar, Srihari Pabbaraja , Srivari Chandrasekhar*
Total synthesis of a thromboxane receptor antagonist, terutroban
Org. Biomol. Chem. 2015, 13, 2951-2957
P. Srihari ,* B. Padmabhavani, S. Ramesh, Y. Bharath Kumar, Ashita Singh, R. Ummanni*
PMA-SiO 2 catalyzed synthesis of indolo[2,3-c]quinolines as potent anti cancer agents
Bioorg. Med. Chem. Lett.2015 , 25, 2360-2365
P. Srihari ,* N. Hari Krishna, Y. Sridhar and Ahmed Kama
A carbohydrate approach for the formal total synthesis of (-)-aspergillide C
Beilstein J. Org. Chem.2014 . I10, 3122-3126
P. Srihari,* N.Harikrishna, Y. Sridhar, A. Krishnam Raju, Ahmed Kamal
An expedient total synthesis of mupirocin H
RSC Advances 2014 , 4,37629-37636
J. S. Yadav*, S. S. Mandal, P. Srihari
Formal total synthesis of Stevastelin B and B3
Helvetica Chim Acta, 2014 , 97, 669-688
Y. Sridhar, P. Srihari *
A Unified Strategy for C1-C14 Fragment of Marinolic acids, Mupirocins, Pseudomonic acids and Thiomarinols: Total Synthesis of Pseudomonic acid methyl monate C
Org. & Biomol. Chem. 2014 , 12, 2950-2959
J. S. Yadav*, Vinay K. Singh, P. Srihari
Formation of substituted tetrahydropyrans through oxetane ring opening: Application to the synthesis of C1-C17 fragment of salinomycin
Org. Lett. 2014 , 16, 836-839
K. Vamshikrishna, G. Srinu, P. Srihari*
A facile chiral pool synthesis of 9-epi-decarestrictine-D, decarestrictine-D and O
Tetrahedron Asymmetry, 2014 , 25, 203-211
A. Sathish Reddy, P. Gangadhar, P. Srihari*
A convergent approach for the total synthesis of a-glucosidase inhibitor (-) panaxjapyne C, (One among the top 25 hottest article during october 2013-december 2013)
Tetrahedron Asymmetry 2013, 24, 1524-1530
A. Sathish Reddy, P. Srihari*
First Total Synthesis of neurotrophic diacetylene petrol (-)-petrosiol D
Tetrahedron Lett. 2013 , 54, 6370-6372
J. S. Yadav*, G. Rajendar, R. Srinivasa Rao, P. Srihari
Total Synthesis of Nhatrangin A
J. Org. Chem. 2013, 7 8, 8524-8530
P. Srihari ,* A. Sathish Reddy, Y. Deepthi, Sashivardhana Kalivendi
First total synthesis and structure confirmation of diactylenic polyol (+)-oploxyne B,
Tetrahedron Lett. 2013, 54, 5616-5618
J. S. Yadav,* G. Rajendar, P. Srihari, B. Sridhar
Short Route to Platencin
Org. Lett. 2013 , 15, 3782-3785
Y. Sridhar, P. Srihari*
The stereoselective approach for the southeast segment (C1-C16) of (+)-sorangicin A
Org. & Biomol. Chem. 2013 , 11, 4640-4645
G. Srinu, P. Srihari*
A catalytic approach for the synthesis of allylic azides from aryl vinyl carbinols
Tetrahedron Lett2013 , 54, 2382-2385
Y. Sridhar, P. Srihari *
Stereodivergent total synthesis of (+)-aspergillide B and (+)-7-epi-aspergillide A
Eur. J. Org. Chem.2013, 578-587
K. Vamshikrishna, P. Srihari*
A conventional approach to the total synthesis of (-)-varitriol and (+)-6'-epivaritriol
Tetrahedron Asymm.2012 , 23, 1584-1587
A. Sathish Reddy, P. Srihari *
A facile approach to the synthesis of securinega alkaloids: stereoselective total synthesis of (-)-allonorsecurinine
Tetrahedron Lett. 2012 , 53, 5926-5928
G. Mehta,* S. Ramesh, P. Srihari, * R. Gajendra Reddy, C. Sumana
Diverted organic Syntehsis (DOS): accessing a new, natural product inspired neurothophically active scaffold through an intramolecular Pauson-Khand reaction
Org. & Biomol. Chem., 2012 , 10, 6830-6833
S. Chandrasekhar,* Ch. Sridhar and P. Srihari
A carbohydrate approach for the formal total synthesis of prostacyclin analogue (16S)-iloprost
Tetrahedron: Asymmetry 2012 , 23(5), 388-394
G. Mehta,* S. Ramesh and P.Srihari *
An enantiodivergent formal synthesis of paecilomycine A
Tetrahedron Lett 2012 , 53, 829-832
K. Vamshikrishna and P. Srihari *
Total synthesis of (+)-varitriol and (+)-6’-epivaritriol
Tetrahedron 2012 , 68, 1540-1546
S.Chandrasekhar,* S NCVL Pushpavalli, Ch. Srinivas, D. Mukhopadhyay, B. Ganganna,K. Vijeender, P. Srihari , Ch. Raji Reddy, M. Janaki Ramaiah and Utpal Bhadra
Aza-flavanones as potent cross-species microRNA inhibitors that arrest cell cycle
Bioorganic & Med. Chem. Lett. 2012 , 22, 645-648
P . Srihari ,* B. Mahankali and K. Rajendraprasad
Stereoselective total synthesis of paecilomycin E
Tetrahedron Lett 2011 , 53, 56-58
P.Srihari,* B Ganganna, K Rajendraprasad, Dinesh C Bhunia and J S Yadav
Bronsted acid catalyzed one-pot condensation of β-naphthol, aldehyde and active methylene substrate: Synthesis of naphthopyrans
Indian Journal of Chemistry 2011 , 50B, 1755-1761
P.Srihari * and Y. Sridhar
Total synthesis of both enantiomers of macrolactone Aspergillide C
Eur. J. Org. Chem.2011 , 33, 6690-6697
J.S. Yadav,* S.S.Mandal, J. S.S. Reddy, P. Srihari
Stereoselective total synthesis of (+)-sapinofuranone B
Tetrahedron 2011,67(25), 4620-4627
J. S. Yadav,* B. Kumaraswamy , A. Sathish Reddy Alugubelli, P . Srihari , Janakiram R Vangala and Shasi V Kalivendi*
Stereoselective total synthesis of (+)-oploxyne A, (-)-oploxyne B and their C-10 epimers and structure revision of natural oploxyne B
J. Org. Chem. 2011, 76 (8), 2568–2576
P. Srihari ,* K. Satyanarayana, B. Ganganna, J. S.Yadav
Formal total synthesis of cyanolide A
J. Org. Chem. 2011, 76, 1922-1925
G. Mehta,* S. Ramesh, P. Srihari
Model studies towards paecilomycine A- C: Exploring scaffold diversity through a key intramolecular Pauson-Khand reaction
Tetrahedron Lett2011 , 52, 1663-1666
S. Chandrasekhar,* P. Srihari , Ch. Nagesh, N. Kiranmai, N. Nagesh, M Mohammed Idris *
Synthesis of readily accessible triazole linked dimer deoxynucleoside phosphoramidite for solid phase oligonucleotide synthesis
Synthesis 2010 , 3710-3714
P. Srihari ,* B. Kumaraswamy, P. Shankar, V. Ravishashidhar, J. S. Yadav
Stereoselective total synthesis of achaetolide and reconfirmation of its absolute configuration
Tetrahedron Lett. 2010 , 51, 6174-6176
A. Ramesh, Y. Sridhar, G. Raju, N. S. Swamy, P. Srihari,* V. Ramesh, R. Srinivas*
Diastereomeric differentiation of two pairs of glucal derivatives by electrospray ionization tandem mass spectrometry
Rapid Communications in Mass Spectrometry, 2010 , 24, 2776-2780
J. S. Yadav,* J. Shyam Sunder Reddy, S. S. Mandal andP. Srihari
Stereoselective total synthesis of (+)-sapinofuranone B
Synlett 2010 ,2636-2638
J. S. Yadav,* G. Rajenar, B. Ganganna, P. Srihari
Stereoselective total synthesis of (+)-polyrhacitide A
Tetrahedron Lett 2010 , 51, 2154-2156
P. Srihari ,* B. Kumaraswamy, G. G. Maheshwara Rao and J. S. Yadav
A stereoselective Aldol approach for the total synthesis of herbarumin I and stagonolide A, (One among the top 25 most cited article 2010-2011)
Synthesis 2010 , (14) 2407-2412
Jhillu Singh Yadav,* Kamani Satyanarayana, Pamu Sreedhar, Pabbaraja Srihari , Thokhir Basha Shaik & Shasi Vardhan Kalivendi
Total synthesis of elegansidiol, farnesiferol B and farnesiferol D
Bioorg. Med. Chem. Lett.2010 , 20, 3814-3817, Corrigendum: Bioorg.Med.Chem Lett 2010 , 20, 6863
P. Srihari ,* B. Kumaraswamy, Dinesh C. Bhunia and J. S. Yadav*
First stereoselective total synthesis of (-)-stagonolide G
Tetrahedron Lett. 2010 , 51, 2903-2905
P. Srihari ,* B. Kumaraswamy, R. Somaiah and J. S. Yadav
The stereoselective total synthesis of (+)-stagonolide B
Synthesis 2010 , (6), 1039-1045
P. Srihari ,* B. Kumaraswamy, G. Maheshwara Rao and J. S. Yadav
First stereoselective total synthesis of (-)-stagonolide A (Hottest article in tetrahedron Asymmetry fro January to March 2010)
Tetrahedron Asymmetry 2010 , (21), 106-111
J. S. Yadav,* B. Thirupathaiah and P. Srihari
A concise stereoselective total synthesis of artemisinin, (Hottest article in tetrahedron fro January to March 2010)
Tetrahedron 2010 , 66, 2005-2009
J. S. Yadav,* E. Vijaya Bhasker, P. Srihari
Synthesis of a key intermediate for the total synthesis of pseudopteroxazole
Tetrahedron 2010 , 66, 1997-2004, Corrigendum: Tetrahedron 2010 , 66, 5295
P. Srihari ,*, Palash Dutta, R. Srinivasa Rao, J. S. Yadav, S. Chandrasekhar, P. Thombare, J. Mohapatra, A. Chatterjee, Mukul R. Jain*
Solvent free synthesis of 1,5-disubstituted tetrazoles derived from Baylis Hillman acetates as potential TNF- a inhibitors
Bio. Med. Chem. Lett. 2009 , 19, 5569–5572
Dinh Hung Mac, Ramesh Samineni, Julien Petrignet, Pabbaraja Srihari , Srivari Chandrasekhar, Jhillu Singh Yadav,* René Grée*
From vinyl Pyranoses to Carbasugars by an iron-catalyzed Reaction complementary to Classical Ferrier Carbocyclisation
Chem. Communications, 2009 , (31), 4717-4719
P. Srihari ,* B. Kumaraswamy and J. S. Yadav
A carbohydrate approach for the synthesis of tetrahydropyran containing C16-C29 fragment of sorangicin A
Tetrahedron 2009 , 65, 6304-6309
J. S. Yadav,* B. Ganganna, Dinesh C. Bhunia, P. Srihari
NbCl 5 mediated deprotection of methoxy methyl ether
Tetrahedron Lett. 2009 , 50, 4318-4320
P. Srihari ,* E. Vijaya Bhasker, A. Bal Reddy, J. S. Yadav
Stereoselective total synthesis of synparvolide B and epi-synparvolide A
Tetrahedron Lett. 2009 , 50, 2420-2424
J. S. Yadav,* Vinay Kumar Singh, Dinesh C Bhunia andP. Srihari
Solvent-free NbCl 5 catalyzed condensation of 1, 3-dicarbonyl compounds and aldehydes: a facile synthesis of trisubstituted alkenes (One among the top 25 hottest article during April -June 2009)
Tetrahedron Lett. 2009 , 50, 2470-2473
P. Srihari ,* Vinay Kumar Singh, Dinesh C Bhunia and J. S. Yadav.
One pot three component coupling reaction: Solvent free synthesis of novel 3-substituted indoles catalyzed by PMA-SiO 2 (One among the top 25 hottest article during April -June 2009)
Tetrahedron Lett. 2009 , 50, 3763-3766
P. Srihari ,* Vinay Kumar Singh, Dinesh C Bhunia and J. S. Yadav
Zinc mediated alkynylation of carbonyl compounds: A facile synthesis of propargyl alcohols
Tetrahedron Lett. 2008 , 49, 7132-7134
P. Srihari ,* G. Rajendar, R. Srinivasa Rao and J. S. Yadav
First stereoselective total synthesis of (+)-dodoneine
Tetrahedron Lett. 2008 , 49, 5590-5592
J. S. Yadav,* V. Naveen Kumar, R. Srinivasa Rao and P. Srihari
A concise stereoselective total synthesis of herbarumin III
Synthesis 2008 , (12), 1938-1942
P. Srihari ,* S. S. Mandal, J. S. S. Reddy, R. Srinivasa Rao and J. S. Yadav
Synthesis of 1,8-dioxo-octahydroxanthenes utilizing PMA-SiO 2 as an efficient reusable catalyst
Chin. Chem. Lett. 2008 , 771-774
P. Srihari ,* S. S. Mandal, J. S. S. Reddy, R. Srinivasa Rao, J. S. Yadav
PMA-SiO 2 catalyzed synthesis of b -keto enol ethers
Chin. Chem. Lett. 2008 , 767-770
P. Srihari ,* J. Shyam Sunder Reddy, S. S. Mandal, K. Satyanarayana and J. S. Yadav
PMA-SiO 2 catalyzed propargylation of aromatic compounds with aryl-propargyl alcohols under solvent free conditions
Synthesis 2008(12), 1853-1860
J. S. Yadav,* A. P. Singh, D. C. Bhunia, A. K. Basak andP. Srihari
A Facile Synthesis of Pyrazolines from Baylis-Hillman Adducts
Chemistry Lett. 2008, 37, 624-625
J. S. Yadav,* G. Kondaji, M. Shiva Ram Reddy and P. Srihari
Facile synthesis of a -iodo carbonyl compounds and a -iodo dimethyl ketals using molecular iodine and trimethylorthoformate
Tetrahedron Lett. 2008, 49, 3810-3813
Alexander Gosslau, Srihari Pabbaraja , Spencer Knapp, and Kuang Yu Chen
Trans- and cis-stilbene polyphenols induced rapid perinuclear mitochondrial clustering and p53- independent apoptosis in cancer cells but not normal cells
European Journal of Pharmacology 2008,587(1-3), 25-34
J. S. Yadav,* P. Sreedhar, P. Srihari , G. Dattatreya Sarma, B. Jagadeesh.
A concise synthesis of a key intermediate for the total synthesis of fumagillin, TNP-470 and ovalicin
Synthesis, 2008, 1460-1466
P. Srihari ,* J. Shyam Sunder Reddy, Dinesh C Bhunia, S. S. Mandal and J. S. Yadav.
PMA-SiO 2 : A heterogenous catalyst for O-, S- and N-nucleophilic substitution reactions of aryl propargyl alcohols
Syn. Commun. 2008, 38, 1448-1455
P. Srihari ,* K. Ravindar, R. Somaiah and J. S. Yadav
First concise total synthesis of 5-epi-prelactone B
Syn. Commun. 38,2008, 1389-1397
P. Srihari ,* Dinesh C. Bhunia, P. Sreedhar, J. S. Yadav
Iodine catalyzed nucleophilic substitution reactions of benzylic alcohols
Synlett 2008 1045-1049
J. S. Yadav,* Dinesh C Bhunia, K. Vamshi krishna and P. Srihari
Niobium(V)pentachloride: An efficient catalyst for C-, N-, O- and S- nucleophilic substitution reactions of benzylic alcohols
Tetrahedron Lett.2007 , 48, 8306-8310
P. Srihari ,* P. Sridhar, Dinesh C Bhunia, J. Shyam Sunder Reddy, S. S. Mandal and J. S. Yadav
Iodine catalyzed C-, and O-nucleophilic substitution reactions of aryl- propargyl methanols
Tetrahedron Lett.2007 , 48, 8120-8124
P. Srihari ,* B. Prem Kumar, K. Subbarayudu and J. S. Yadav
A convergent approach for the total synthesis of (-)-synrotolide diacetate
Tetrahedron Lett.2007, 48, 6977-6981
J. S. Yadav,* A. K. Basak and P. Srihari
An Aldol Approach to the Synthesis of Anti-tubercular Erogorgiaene
Tetrahedron Lett.2007 , 48, 2841-2843
P. Srihari ,* Ashutosh Pratap Singh, A. K. Basak & J. S. Yadav
Zinc mediated propenylation of Baylis Hillman acetates
Tetrahedron Lett.2007 , 48, 5999-6001
Jhillu Singh Yadav,* Sreedhar Pamu, Dinesh Chandra Bhunia, Srihari Pabbaraja
Formal total synthesis of Ovalicin by carbohydrate approach
Synlett, 2007 , 992-994
P. Srihari ,* E. Vijaya Bhasker, S. J. Harshavardhan and J. S. Yadav
Stereoselective Total Synthesis of iso-Cladospolide B
Synthesis 2006 , 4041-4045
P. Srihari ,* Ashutosh pratap singh, Ruchi Jain, and J. S. Yadav
A Facile nucleophilic displacement of Baylis Hillman Acetates with Ammonium Thiocyanate
Synthesis, 2006 , 2772-2776
P. Srihari ,* Y. Srinivasa Rao, Debjit Basu and S. Chandrasekhar
Tris(pentafluorophenyl)borane-catalyzed synthesis of N-Benzyl Pyrrolidines
Synthesis, 2006 , 2646-2648
S Chandrasekhar,* G. Chandrasekhar, M. Srinivasa Reddy and P. Srihari
A facile and chemoselective conjugate reduction using polymethylhydroxiloxane (PMHS) and catalytic B(C 6 F 5 ) 3
Org. Bio. Chem. 2006 , 19, 1650-1652.
S. Knapp,* C. Yang, P. Srihari , B.Rempel,S. Reid, S. G. Withers
Synthesis and Kinetic Analysis of the N-Acetylhexosaminidase Inhibitor XylNAc-Isofagomine
J. Org. Chem. 2005 , 70 (19), 7715-7720.
S. Chandrasekhar,* B. Nagendra Babu, Moinuddin Ahmed, M. Venkat Reddy, P. Srihari , B. Jagadeesh, A. Prabhakar
Safe and conveninet reduction of D 2-Isoxazolines with PMHS,Pd(OH) 2 /C
Synlett, 2004 , 7, 1303-1305.
J. S. Yadav* and P. Srihari
Formal total synthesis of Salicylihalamides A & B
Tetrahedron Asymmetry 2004 15(1), 81-89
G. Sabitha,* Ch.Srinivas, P.Srihari and J. S. Yadav
Stereoselective Total Synthesis of (+) Virol C
Synthesis 2003 , (17), 2699-2704
S. Chandrasekhar,* Ch. Srinivas and P. Srihari
Phenyl sulphonyl acetaldehyde diethyl acetal: A new robust 1, 2-diol protective group
Synthetic Communications, 2003 , 6, 895-902
J. S. Yadav,* B. V. Subba Reddy, Ch. Srinivas and P. Srihari
Ultrasound-promoted deoxygenation of sulphoxides by samarium – NH 4 Cl
Synlett, 2001 , 854-856
J. S. Yadav,* B. V. Subba Reddy and P. Srihari
Scandium triflate catalyzed allylation of acetals and gem-diacetates: A facile synthesis of homoallyl ethers and acetates
Synlett. 2001 , 673-675
J. S. Yadav,* B. V. Subba Reddy, Sushil Kumar Pandey, P. Srihari and I. Prathap
Scandium triflate catalyzed 1, 3-dipolar cycloaddition of aziridines with alkenes
Tetrahedron Lett. 2001 , 42, 9089-9092
S. Chandrasekhar,* G. Rajaiah and P. Srihari
New and practical synthesis of 1, 4-dihydro benzopyrano pyrazoles
Tetrahedron Lett. 2001 , 37, 6599-6601