104) Synthesis of 2‐Chloro‐3‐amino indenone derivatives and their evaluation as inhibitors of DNA dealkylation repair
Richa Nigam, Kaki Raveendra Babu, Topi Ghosh, Bhavini Kumari, Prolay Das, Roy Anindya, Faiz Ahmed Khan, 2021, Chemical Biology & Drug Design, 97, 6, 1170-1184
DOI:10.1111/cbdd.13839
103) Synthesis and antibacterial activities of marine natural product ianthelliformisamines and subereamine synthetic analogues
Shivaji Narayan Khadake, Shaik Karamathulla, Tapan Kumar Jena, Mohan Monisha, Nikhil Kumar Tuti, Faiz Ahmed Khan, Roy Anindya, 2021, Bioorganic & Medicinal Chemistry Letters, 39, 127883
DOI:10.1016/j.bmcl.2021.127883
102) Symmetrical and un-symmetrical curcumin analogues as selective COX-1 and COX-2 inhibitor
Monisha Mohan, Mulla Althafh Hussain, Faiz Ahmed Khan, Roy Anindya, 2021, European Journal of Pharmaceutical Sciences,160, 105743
DOI:10.1016/j.ejps.2021.105743
101) Synthesis of 2-Chloro-3-amino indenone derivatives and their evaluation as inhibitors of DNA dealkylation repair
Anindya Roy, Faiz Ahmed Khan, 2021, John Wiley and Sons Inc
100) FeCl3 catalyzed intermolecular reaction between enol ethers and anilines: Access to 2, 3-substituted indoles through aryl group migration
Tapan Kumar Jena, Faiz Ahmed Khan, 2020, Tetrahedron Letters, 61, 49,152583
DOI:10.1016/j.tetlet.2020.152583
99) Brønsted acid-induced synthesis of methyl benzofurans via Grob type fragmentation of norbornyl derivatives
Kadavergu Sravanthi, Faiz Ahmed Khan, 2020, Tetrahedron Letters, 61, 38, 152351
DOI:10.1016/j.tetlet.2020.152351
98) Total Synthesis of (±)-Cassumunins A–C and Curcumin Analogues
Mulla Althafh Hussain, Faiz Ahmed Khan, 2020, synthesis, 52, 10, 1561-1575
DOI: 10.1055/s-0039-1690794
97) Acid mediated synthesis of thiazolines, thiazoles and enamide derivatives from methyl enol ethers: Application towards synthesis of wilsoniamine B
Tapan Kumar Jena, Faiz Ahmed Khan, 2020, Tetrahedron Letters, 61, 13, 151675
DOI:10.1016/j.tetlet.2020.151675
96) FeCl3 catalyzed 1, 6-conjugate addition of phenol C-nucleophiles: Facile synthesis of diarylmethanes
Kukkamudi Sreenivas, Faiz Ahmed Khan, 2020, Tetrahedron, 76, 6,130885
DOI:10.1016/j.tet.2019.130885
95) Total Synthesis of Enisorine D and its Analogues
Shashi Shashi, Mulla Althafh Hussain, Faiz Ahmed Khan, 2019, Synthesis, 51, 24, 4601-4610
DOI: 10.1055/s-0039-1690025
94) Direct α-Benzylation of Methyl Enol Ethers with Activated Benzyl Alcohols: Its Rearrangement and Access to (±)-Tetrahydronyasol, Propterol A, and 1, 3-Diarylpropane
Tapan Kumar Jena, Faiz Ahmed Khan, 2019, The Journal of Organic Chemistry, 84, 21, 14270-14280
DOI:10.1021/acs.joc.9b02064
93) Total synthesis of (±) aspidostomide B, C, regioisomeric N-methyl aspidostomide D and their derivatives
Mulla Althafh Hussain, Faiz Ahmed Khan, 2019, Tetrahedron Letters, 60,151040
92) 1, 6-Conjugate addition of C-nucleophiles to p-quinone methide surrogate: Synthesis of diarylpropanes
Kukkamudi Sreenivas, Faiz Ahmed Khan, 2019, Tetrahedron, 75, 633-642
DOI:10.1016/j.tet.2018.12.048
91) Indenone derivatives as inhibitor of human DNA dealkylation repair enzyme AlkBH3
Richa Nigam, Kaki Raveendra Babu, Topi Ghosh, Bhavini Kumari, Deepa Akula, Subha Narayan Rath, Prolay Das, Roy Anindya, Faiz Ahmed Khan, 2018, Organic and Medicinal Chemistry, 26, 4100-4112
DOI:10.1016/j.bmc.2018.06.040
90) An unexpected acid mediated rearrangement of monoethylene ketal of 2-methyl-2-(3-methylbut-2-en-1-yl)cyclohex-4-ene-1,3-diones to chromane
Kukkamudi Sreenivas, Faiz Ahmed Khan, 2018, Tetrahedron Letters, 59, 1244-1248
DOI:10.1016/j.tetlet.2018.02.045
89) Synthesis of γ-butyrolactone fused cyclooctene
G Hari Mangeswara Rao, Faiz Ahmed Khan, 2018, synthetic communications, 48, 3, 318-322
DOI:10.1080/00397911.2017.1401638
88) N-dealkylative SNAr reaction using aromatic halides: Synthesis of dihydrobenzoxazine and tetrahydrobenzoxazepine derivatives
Mosim Amin Pathan, Faiz Ahmed Khan, 2017, Tetrahedron, 73, 6008-6020
DOI:10.1016/j.tet.2017.08.047
87) Synthesis of carbazole analogs via Grob fragmentation of norbornyl α-diketones
Kadavergu Sravanthi, Sumit Kumar Agrawal, Chintada Nageswara Rao, Faiz Ahmed Khan, Tetrahedron Lettets, 57,31,3449-4352
DOI: 10.1016/j.tetlet.2016.06.080
86) Aromaticity driven 1, 6-conjugate addition of amines and phenols to cyclohexadienone derivative
Kaki Raveendra Babu, Faiz Ahmed Khan, Tetrahedron, 2016, 72(5), 699-705
DOI:10.1016/j.tet.2015.12.019
85) Synthesis of platencin core structures via twist-brendane.
Faiz Ahmed Khan, Basavaraj M Budanur, Arkivoc, 2016
DOI:10.3998/ark.5550190.p009.333
2015
84) Superoxide mediated isomerization of 4-aryl-but-1-ynes to 1-aryl-1,3-butadienes
Faiz Ahmed Khan, Basavaraj M. Budanur, Tetrahedron, 2015, (Accepted Manuscript)
DOI: 10.1016/j.tet.2015.07.075
83) Effect of bridgehead substitution in the Grob fragmentation of norbornyl ketones: A new route to substituted halophenols
Sumit Choudhury, Saeed Ahmad and Faiz Ahmed Khan, Org. Biomol. Chem., 2015, (Accepted Manuscript)
DOI: 10.1039/C5OB01287B
82) BF3-Et2O mediated skeletal rearrangements of norbornyl appended cyclopentanediols
Chintada Nageswara Rao and Faiz Ahmed Khan, Org. Biomol. Chem., 2015,13,2768.
DOI:10.1039/c4ob02423k
81) An unusual formation of diarylmethane scaffolds from 4-(halomethyl)cyclohex-2-enone derivatives
K. R. Babu and F. A. Khan. Tetrahedron Lett., 2015, 56, 4067-4070.
DOI:10.1016/j.tetlet.2015.04.128
80) Synthesis of marine brominated alkaloid amathamide F: A palladium-catalyzed enamide synthesis
S. Ahmad, S. Choudhury and F. A. Khan, Tetrahedron, 71, 2015, 4192-4202.
DOI:10.1016/j.tet.2015.04.091
79) A short, general, Suzuki-Miyaura coupling anchored approach to 3-alkenylbutenolides: total synthesis of akolactones A & B, hamabiwalactone B and ancepsenolide
L. Vasamsetty, F. A. han and G. Mehta. Tetrahedron, 71, 2015, 3209-3215.
DOI:10.1016/j.tet.2015.04.009
78) Bridgehead Substitution via Putative Norborn-1-en-3-ones: Application in the Synthesis of Complex Molecules
F. A. Khan, B. M. Budanur and C. Sudheer. Chem. Eur. J., 2015, 21, 7021-7025.
DOI:10.1002/chem.201500131
77) A domino reaction of tetrahalo-7,7-dimethoxybicyclo[2.2.1]heptenyl alcohols leading to indenones and a de novo synthesis of ninhydrin derivatives
Babu, K. R.; Khan, F. A. Org. Biomol. Chem., 2015,13,299-308.
DOI:10.1039/C4OB01977F
76) Diastereoselective Synthesis of Spirocyclic Dihydrofurans and 1-Oxaspiro[4.5]decan-6-one Derivatives from Norbornyl alpha-Diketones
Mahadevegowda, S. H.; Khan, F. A. Eur. J. Org. Chem. 2015,4, 858-870.DOI: 10.1002/ejoc.201403087
DOI:10.1002/ejoc.201403087
2014
75) A model approach towards the polycyclic framework present in cembranoid natural products dissectolide A, plumarellide and mandapamate
Vasamsetty, L.; Khan, F. A.; Mehta, G. Tetrahedron Lett. 2014, 55, 7068-7071.
DOI:10.1016/j.tetlet.2014.10.141
74) Superoxide chemistry revisited: synthesis of tetrachloro-substituted methylenenortricyclenes
Budanur, B. M.; Khan, F. A. Beilstein J. Org. Chem. 2014, 10, 2531-2538.
DOI:10.3762/bjoc.10.264
73) Total synthesis of novel bioactive natural product paracaseolide A and analogues: computational evaluation of a proposed biomimetic Diels-Alder reaction
Vasamsetty, L.; Sahu, D.; Ganguly, B.; Khan, F. A.; Mehta, G. Tetrahedron, 2014, 70, 8488-8497.
DOI:10.1016/j.tet.2014.09.072
72) A solvent effect in the reaction of diazomethane with norbornane-2,3-dione 3-hemiketals
Rao, G. H. M.; Khan, F. A. Synth. Commun. 2014, 44, 3314.
DOI:10.1080/00397911.2014.926554
71) Total syntheses of (�)-cis- and (�)-trans-neocnidilides
Mahadevegowda, S. H.; Khan, F. A. Tetrahedron Lett. 2014, 55, 4400.
DOI:10.1016/j.tetlet.2014.06.007
70) Syntheses of a library of molecules on the marine natural product ianthelliformisamines platform and their biological evaluation
Khan, F. A.; Ahmad, S., Kodipelli, N.; Shivange, G.; Anindya, R. Org. Biomol. Chem. 2014, 12, 3847.
DOI : 10.1039/c3ob42537a
This article selected as inside front cover of the issue.
69) Synthesis of the tetrahydrofuran unit of varitriol and gama- butyrolactones from 5-oxabicyclo[2.1.1]hexane derivative via oxidative cleavage reactions
Mahadevegowda, S. H.; Khan, F. A. Tetrahedron Lett. 2014, 55, 2266.
DOI : 10.1016/j.tetlet.2014.02.082
2013
68) An unusual fragmentation of oxetane-embedded tetracyclic ketal systems
Rao, G. H. M.; Khan, F. A. J. Org. Chem. 2013, 21, 11092.
DOI : 10.1021/jo401870s
67) Grob-type fragmentation of 5-oxabicyclo[2.1.1]hexane system: A strategy for synthesis of annulated and 2,2,5-trisubstituted tetrahydrofurans
Mahadevegowda, S. H.; Khan, F. A. Tetrahedron 2013, 69, 8494.
DOI : 10.1016/j.tet.2013.07.005
66) Total synthesis of a novel oxa-bowl natural product paracaseolide A via a 'putative' biomimetic pathway
Vasamsetty, L.; Khan, F. A.; Mehta, G. Tetrahedron Lett., 2013, 54, 3522.
DOI : 10.1016/j.tetlet.2013.04.097
65) Synthesis of wilsoniamines A and B
Khan, F. A.; Ahmad, S. Tetrahedron Lett. 2013, 54, 2996.
DOI : 10.1016/j.tetlet.2013.03.122
2012
64) Synthesis of reported and revised structures of amathamide D and synthesis of convolutamine F, H and lutamide A, C
Khan, F. A.; Ahmad, S. J. Org. Chem. 2012, 77, 2389.
DOI : 10.1021/jo3000173
2011
63) An efficient synthesis of a cyclopentannulated pyrrolidine derivative
Khan, F. A.; Upadhyay, S. K. Synthesis. 2011, 2423.
DOI : 10.1055/s-0030-1260114
62) Grob fragmentation of norbornyl alpha-diketones: A route to alpha-ketoenols and aromatic compounds
Khan, F.A.; Rao, C.N. J. Org. Chem. 2011, 76, 3320.
DOI : 10.1021/jo200223a
2010
61) Synthesis and thermal properties of rigid oxa-bridged-containing dimers and tetramers
Khan, F. A.; Parasuraman, K., Donnio, B. Tetrahedron 2010, 66, 8745.
DOI : 10.1016/j.tet.2010.09.003
60) Synthesis of oxa-bridged derivatives from Diels-Alder bis-adducts of butadiene and 1,2,3,4-tetrahalo-5,5-dimethoxycyclopentadiene
Khan, F. A.; Parasuraman, K. Beilstein J. Org. Chem. 2010, 6, 64.
DOI : 10.3762/bjoc.6.64
59) Synthesis and electrochemical properties of substituted para-benzoquinone derivatives
Khan, F. A.; Choudhury, S. Tetrahedron Lett. 2010, 51, 2541.
DOI : 10.1016/j.tetlet.2010.03.007
58) An efficient synthesis of substituted meta-halophenols and their methyl ethers: insight into the reaction mechanism
Khan, F. A.; Choudhury, S. Eur. J. Org. Chem. 2010, 15, 2954.
DOI : 10.1002/ejoc.201000071
2009
57) Synthesis and electrochemical signature of novel norbornyl-ferrocene hybrids
Khan, F. A.; Upadhyay, S. K. Synthesis 2009, 16, 2773.
DOI : 10.1055/s-0029-1217601
56) Synthesis of 9-oxa-noradamantane derivative, an aesthetically pleasing 'oxa-basket'
Khan, F. A.; Rao, Ch. N. Tetrahedron Lett. 2009, 50, 5751.
DOI : 10.1016/j.tetlet.2009.07.143
55) Oxygen as moderator in the zinc-mediated reduction of aromatic nitro to azoxy compounds
Khan, F. A.; Sudheer, Ch. Tetrahedron Lett. 2009, 50, 3394.
DOI : 10.1016/j.tetlet.2009.02.122
54) Azacrown-oxabridged macrocycle: A novel hybrid fluorogenic chemosensor for transition and heavy metal ions
Khan, F. A.; Parasuraman, K.; Sadhu, K. K. Chem. Commun. 2009, 17, 2399.
DOI : 10.1039/B820479A
53) An Efficient method for zinc mediated reduction of norbornyl alpha-diketones in [bmim][BF4]:H2O
Khan, F. A.; Sudheer, Ch. Arkivoc, 2009, 7, 222.
DOI : http://dx.doi.org/10.3998/ark.5550190.0010.721
52) Ruthenium-mediated oxidation under buffered conditions: A simple and useful protocol for the synthesis of norbornyl alpha-diketones with acid sensitive functionalities
Khan, F. A.; Sudheer, Ch. Adv. Synth. Catal. 2009, 351, 939.
DOI : 10.1002/adsc.200900042
2008
51) A chiral pool approach to the synthesis of optically active tetrahalo norbornyl building blocks
Khan, F. A.; Sudheer, Ch. Org. Lett. 2008, 10, 3029.
DOI : 10.1021/ol800990m
50) A stereoselective C7nC5x free-radical cascade route to optically pure and potentially useful tetracyclic amines
Khan, F. A.; Upadhyay, S. K. Tetrahedron Lett. 2008, 49, 6111.
DOI : 10.1016/j.tetlet.2008.08.013
2007
49) Lead(IV) acetate: Intriguing reactivity profile
Khan, F. A.; Sudheer, Ch.; Soma, L. Chem. Commun. 2007, 41, 4239.
DOI : 10.1039/b708268a
48) A formal total synthesis of (�)-neplanocin A
Khan, F. A.; Rout, B. J. Org. Chem. 2007, 72, 7011.
DOI : 10.1021/jo0710127
47) Synthesis of highly functionalized delta-lactone-fused cyclopentanoids
Khan, F. A.; Krishnakumar, K. S.; Sudheer, Ch. Synthesis, 2007, 1054.
DOI : 10.1055/s-2007-965948
46) Serendipitously discovered diazomethane-mediated novel molecular rearrangements of norbornyl alpha-ketohemiketals
Khan, F. A.; Rao, G. H M.; Satapathy, R.; Parasuraman, K. Org. Lett. 2007, 9, 1581.
DOI : 10.1021/ol070442g
45) Synthesis of a novel, bowl-like bis gamma-lactone
Khan, F. A.; Dwivedi, V.; Rout, B. Tetrahedron Lett. 2007, 48, 207.
DOI : 10.1016/j.tetlet.2006.11.062
44) Synthesis of tribromobenzofuran and tribromobenzopyran derivatives from methyl 2-allyl-4,5,6-tribromo-3-hydroxybenzoate
Khan, F. A.; Soma, L. Tetrahedron Lett. 2007, 48, 85.
DOI : 10.1016/j.tetlet.2006.11.005
2006
43) An efficient synthesis of diquinane-based bis-gamma-lactones
Khan, F. A.; Nageswara Rao, Ch. Tetrahedron Lett. 2006, 47, 7567
DOI : 10.1016/j.tetlet.2006.08.092
42) Benzannulated cyclooctanol derivatives by samarium diiodide induced intramolecular carbonyl-alkene coupling-Scope, limitations, stereoselectivity
Reissig, H.-U.; Khan, F. A.; Czerwonka, R.; Dinesh, C. U.; Shaikh, A. L.; Zimmer, R. Eur. J. Org. Chem. 2006, 4419.
DOI : 10.1002/ejoc.200600360
41) Total synthesis of (�)-pentenomycin
Khan, F. A.; Rout, B. Tetrahedron Lett. 2006, 47, 5251.
DOI : 10.1016/j.tetlet.2006.05.156
40) An efficient route to pentasubstituted phenols
Khan, F. A.; Choudhury, S. Eur. J. Org. Chem. 2006, 672.
DOI : 10.1002/ejoc.200500603
2005
39) A new reaction of diazomethane with norbornyl alpha-diketones
Khan, F. A.; Satapathy, R.; Sudheer, Ch.; Rao, Ch. N. Tetrahedron Lett. 2005, 46, 7193.
DOI : 10.1016/j.tetlet.2005.08.087
38) Concise synthesis of novel oxa-bridged compounds
Khan, F. A.; Dash, J.; Sudheer, Ch.; Sahu, N.; Parasuraman, K. J. Org. Chem. 2005, 70, 7565.
DOI : 10.1021/jo0507385
37) Highly efficient and recyclable ruthenium-based supported catalysts
Khan, F. A.; Sahu, N. J. Catal.2005, 438.
DOI : 10.1016/j.jcat.2005.02.001
36) 1-Butyl-3-methyl-imidazolium tetrafluoroborate as a recyclable reaction medium for henry reaction
Khan, F.A.; Sudheer, Ch.; Sahu, N. Synth. Commun. 2005, 35, 201.
DOI : 10.1081/SCC-200048415
2004
35) A short and stereoselective synthesis of functionalized pentenomycin derivatives
Khan, F. A.; Dash, J.; Rout, B. Tetrahedron Lett. 2004, 45, 9285.
DOI : 10.1016/j.tetlet.2004.10.065
34) A rapid and stereoselective route to the trans-hydrindane ring system
Khan, F. A.; Satapathy, R.; Dash, J.; Savitha, G. J. Org. Chem. 2004, 69, 5295.
DOI : 10.1021/jo049615v
33) Diastereoselection during allylindium addition to norbornyl alpha-diketones
Khan, F. A.; Dash, J. Eur. J. Org. Chem. 2004, 2692.
DOI : 10.1002/ejoc.200400044
32) Indium-mediated regio- and diastereoselective reduction of norbornyl alpha-diketones
Khan, F. A.; Dash, J.; Sudheer, Ch. Chem.-Eur. J. 2004, 10, 2507.
DOI : 10.1002/chem.200305656
31) Hydrotalcite catalysis in ionic liquid medium: A recyclable reaction system for heterogeneous Knoevenagel and nitroaldol condensation
Khan, F. A.; Dash, J.; Satapathy, R.; Upadhyay, S. K. Ch. Tetrahedron Lett. 2004, 45, 3055.
DOI : 10.1016/j.tetlet.2004.02.103
2003
30) Chemoselective reduction of aromatic nitro and azo compounds in ionic liquids using zinc and ammonium salts
Khan, F. A.; Dash, J.; Sudheer, Ch.; Gupta, R. K. Tetrahedron Lett. 2003, 44, 7783.
DOI : 10.1016/j.tetlet.2003.08.080
29) A novel and expeditious approach to unusual spirolactam building blocks
Khan, F. A.; Dash, J. J. Org. Chem. 2003, 68, 4556.
DOI : 10.1021/jo034023i
2002
28) An easy access to gamma-lactone-fused cyclopentanoids
Khan, F. A.; Dash, J.; Sahu, N.; Sudheer, Ch. J. Org. Chem. 2002, 67, 3783.
DOI : 10.1021/jo025521e
27) Regio- and diastereoselective reduction of nonenolizable alpha-diketones to acyloins mediated by indium metal
Khan, F. A.; Dash, J.; Sahu, N.; Gupta, S. Org. Lett. 2002, 4, 1015.
DOI : 10.1021/ol025593s
26) Synthesis of a novel, highly symmetric bis-oxa-bridged compound
Khan, F. A.; Dash, J. J. Am. Chem. Soc. 2002, 124, 2424.
DOI : 10.1021/ja017371f
2001
25) Rearrangement of 1,4,5,6-tetrahalo-7,7-dimethoxybicyclo[2.2.1]-hept-5-en-2-ones to phenolic derivatives
Khan, F. A.; Dash, J.; Jain, D.; Prabhudas, B. J. Chem. Soc., Perkin Trans. 1, 2001, 3132
DOI : 10.1039/B108152G
24) Synthesis of novel caged bis-hemiacetals and their facile conversion to symmetric bis-alpha-halo-gamma-lactones
Khan, F. A.; Sahu, N.; Dash, J.; Prabhudas, B. J. Indian Inst. Sci. 2001, 81, 325.
2000
23) Pd-catalyzed reactions of donor-Acceptor-substituted cyclopropanes and their ring-opened derivatives: Attempted heck cyclization and novel one-pot enolate arylations
Khan, F. A.; Czenvonka, R.; Reissig, H.-U. Eur. J. Org. Chem. 2000, 3607.
DOI : 10.1002/1099-0690(200011)2000:21<3607::AID-EJOC3607>3.0.CO;2-N
22) A ruthenium-catalyzed, novel and facile procedure for the conversion of vicinal dihaloalkenes to alpha-diketones
Khan, F. A.; Prabhudas, B.; Dash, J.; Sahu, N. J. Am. Chem. Soc. 2000, 122, 9558.
DOI : 10.1021/ja001956c
21) Indium-mediated, highly efficient and diastereoselective addition of cyclic secondary allylic bromides to carbonyl compounds
Khan, F. A.; Prabhudas, B. Tetrahedron, 2000, 56, 7595.
DOI : 10.1016/S0040-4020(00)00672-4
20) Palladium-catalyzed reactions of allenes
Zimmer, R.; Dinesh, C. U.; Nandanan, E.; Khan, F. A. Chem. Rev. 2000, 100, 3067.
DOI : 10.1021/cr9902796
19) 1,2,3,4-Tetrachloro-5,5-dimethoxy-cyclopenta-1,3-diene: Diels-Alder reactions and applications of the products formed.
Khan, F. A.; Prabhudas, B.; Dash, J. J. prakt. Chem., 2000, 342, 512.
DOI : 10.1002/1521-3897(200006)342:5<512::AID-PRAC512>3.0.CO;2-V
1999
18) A simple and preparatively useful tributylstannane mediated selective reduction and bridgehead functionalization of tetrahalonorbornene derivatives
Khan, F. A.; Prabhudas, B. Tetrahedron Lett. 1999, 40, 9289.
DOI : 10.1016/S0040-4039(99)01948-6
Publications During Postdoctoral and Doctoral Research Carrier
17) Configurational analysis of 14,14-dimethyl-12-oxatricyclo[9.2.1.03,8]tetradeca-3,5,7-trien-13-one
Zimmer, R.; Zahn, G.; Khan, F. A.; Reissig, H.-U. Acta Cryst. 1999, C55, 1941.
DOI : doi:10.1107/S0108270199009014
16) A novel Sm(II)-induced route to highly substituted benzannulated cyclooctanol derivatives
Khan, F. A.; Czerwonka, R.; Zimmer, R.; Reissig, H.-U. Synlett, 1997(8), 995.
DOI : 10.1055/s-1997-934
15) Samarium diiodide. A mild and selective reagent in organic synthesis
Khan, F. A.; Zimmer, R. J. Prakt. Chem., 1997, 339: 101.
DOI : 10.1002/prac.19973390120
14) pi-Face selectivities in nucleophilic additions to 2-endo-arylnorbornan-7-ones: the role of through-space electrostatic interactions
Mehta, G.; Khan, F. A.; Mohal, N.; Namboothiri, I. N. N.; Kalyanaraman, P.; Chandrasekhar, J. Chem. Soc., Perkin Trans. 1, 1996, 2665.
DOI : 10.1039/P19960002665
13) A novel Pd(0)-catalyzed one-pot transformation of substituted siloxycyclopropanes to indane derivatives
Khan, F. A.; Czerwonka, R.; Adcock, W. Synlett, 1996 (6), 533.
DOI : 10.1055/s-1996-5483
12) Electrostatic vs. orbital effects as stereoinductive factors in nucleophilic additions to the endo-substituted norbornan-7-one ring system
Mehta, G.; Khan, F. A.; Czerwonka, R.; Reissig, H.-N. J. Chem. Soc., Perkin Trans. 2, 1995, 2189.
DOI : 10.1039/P29950002189
11) pi-Facial diastereoselection in reductions of sterically unbiased ketones containing the norbornyl framework: further tests for theoretical models
Mehta, G.; Khan, F. A.; Ganguly, B.; Chandrasekhar, J. J. Chem. Soc., Perkin Trans. 2, 1994, 2275.
DOI : 10.1039/P29940002275
10) Electrostatic vs. orbital control of facial selectivities in pi Systems: Experimental and theoretical study of electrophilic additions to 7-isopropylidenenorbornanes
Mehta, G.; Khan, F. A.; Gadre, S. R.; Shirsat, R. N.; Ganguly, B.; Chandrasekhar, J. Angew. Chem. Int. Ed. 1994, 33, 1390.
DOI : 10.1002/anie.199413901
9) A simple computational model for predicting pi-facial selectivity in reductions of sterically unbiased ketones. Relative importance of electrostatic and orbital interactions
Ganguly, B.; Chandrasekhar, J.; Khan, F. A.; Mehta, G. J. Org. Chem. 1993, 58, 1734.
DOI : 10.1021/jo00059a022
8) Short, convenient preparative procedures for 7-isopropylidenenorbornane, 7-isopropylidenenorbornene and 7- isopropylidenenorbornadiene
Mehta, G.; Khan, F. A. Synth. Commun. 1993, 23(21), 2985.
DOI : 10.1080/00397919308011141
7) Long-range substituent effects on the regioselectivity of one-carbon ring expansion of norbornan-7-ones
Mehta, G.; Khan, F. A. J. Chem. Soc., Perkin Trans. 1, 1993, 1727.
DOI : 10.1039/P19930001727
6) Importance of orbital and electrostatic interactions in determining pi-facial selectivities in nucleophilic additions to endo-substituted bicyclo[2.2.2]octan-2-ones
Mehta, G.; Khan, F. A.; Ganguly, B.; Chandrasekhar, J. J. Chem. Soc., Chem. Commun., 1992, 1711.
DOI : 10.1039/C39920001711
5) Modification of pi-face selectivity of 7-norbornenones during reduction in b-cyclodextrin and solid state
Mehta, G.; Khan, F. A.; Lakshmi, K. A. Tetrahedron Lett. 1992, 33, 7977.
DOI : 10.1016/S0040-4039(00)74793-9
4) Modulation of pi-facial selectivities in nucleophilic additions to 7-norbornenones
Mehta, G.; Khan, F. A. Tetrahedron Lett. 1992, 33, 3065.
DOI : 10.1016/S0040-4039(00)79601-8
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