Click Sl.No. for the link to the particular paper
157
Stereoselective Synthesis of Protected 12-Membered Macrolide Antibiotic 13E-Disciformycin B Aglycone
Naresh Gantasala, Sankara Rao Patta, Srihari Pabbaraja*
Eur. J. Org. Chem. 2025, XXX-XXX
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