| Year |
Citation |
Score |
| 2021 |
Asma Ziya Ahmad S, Jena TK, Khan FA. Alkyl Enol Ethers: Development in Intermolecular Organic Transformation. Chemistry, An Asian Journal. PMID 33979009 DOI: 10.1002/asia.202100277 |
0.339 |
|
| 2020 |
Hussain MA, Khan FA. Total Synthesis of (±)-Cassumunins A–C and Curcumin Analogues Synthesis. 52: 1561-1575. DOI: 10.1055/S-0039-1690794 |
0.459 |
|
| 2020 |
Sravanthi K, Khan FA. Brønsted acid-induced synthesis of methyl benzofurans via Grob type fragmentation of norbornyl derivatives Tetrahedron Letters. 61: 152351. DOI: 10.1016/J.Tetlet.2020.152351 |
0.441 |
|
| 2020 |
Jena TK, Khan FA. Acid mediated synthesis of thiazolines, thiazoles and enamide derivatives from methyl enol ethers: Application towards synthesis of wilsoniamine B Tetrahedron Letters. 61: 151675. DOI: 10.1016/J.Tetlet.2020.151675 |
0.475 |
|
| 2020 |
Sreenivas K, Khan FA. FeCl3 catalyzed 1,6-conjugate addition of phenol C-nucleophiles: Facile synthesis of diarylmethanes Tetrahedron. 76: 130885. DOI: 10.1016/J.Tet.2019.130885 |
0.527 |
|
| 2019 |
Jena TK, Khan FA. Direct α-Benzylation of Methyl Enol Ethers with Activated Benzyl Alcohols: Its rearrangement and Access to (±)-Tetrahydronyasol, Propterol A and 1,3-Diarylpropane. The Journal of Organic Chemistry. PMID 31545892 DOI: 10.1021/Acs.Joc.9B02064 |
0.455 |
|
| 2019 |
Shashi S, Hussain MA, Khan FA. Total Synthesis of Enisorine D and its Analogues Synthesis. 51: 4601-4610. DOI: 10.1055/S-0039-1690025 |
0.391 |
|
| 2019 |
Hussain MA, Khan FA. Total synthesis of (±) aspidostomide B, C, regioisomeric N-methyl aspidostomide D and their derivatives Tetrahedron Letters. 60: 151040. DOI: 10.1016/J.Tetlet.2019.151040 |
0.435 |
|
| 2019 |
Sreenivas K, Khan FA. 1,6-Conjugate addition of C-nucleophiles to p-quinone methide surrogate: Synthesis of diarylpropanes Tetrahedron. 75: 633-642. DOI: 10.1016/J.Tet.2018.12.048 |
0.475 |
|
| 2018 |
Nigam R, Babu KR, Ghosh T, Kumari B, Akula D, Rath SN, Das P, Anindya R, Khan FA. Indenone derivatives as inhibitor of human DNA dealkylation repair enzyme AlkBH3. Bioorganic & Medicinal Chemistry. PMID 30041948 DOI: 10.1016/J.Bmc.2018.06.040 |
0.601 |
|
| 2018 |
Rao GHM, Khan FA. Synthesis of γ-butyrolactone fused cyclooctene Synthetic Communications. 48: 318-322. DOI: 10.1080/00397911.2017.1401638 |
0.403 |
|
| 2018 |
Sreenivas K, Khan FA. 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 Tetrahedron Letters. 59: 1244-1248. DOI: 10.1016/J.Tetlet.2018.02.045 |
0.336 |
|
| 2017 |
Pathan MA, Khan FA. N-dealkylative SNAr reaction using aromatic halides: Synthesis of dihydrobenzoxazine and tetrahydrobenzoxazepine derivatives Tetrahedron. 73: 6008-6020. DOI: 10.1016/J.Tet.2017.08.047 |
0.445 |
|
| 2016 |
Khan FA, Budanur BM. Synthesis of platencin core structures via twist-brendane Arkivoc. 2016. DOI: 10.3998/Ark.5550190.P009.333 |
0.377 |
|
| 2016 |
Sravanthi K, Agrawal SK, Rao CN, Khan FA. Synthesis of carbazole analogs via Grob fragmentation of norbornyl α-diketones Tetrahedron Letters. 57: 3449-3452. DOI: 10.1016/J.Tetlet.2016.06.080 |
0.489 |
|
| 2016 |
Babu KR, Khan FA. Aromaticity driven 1,6-conjugate addition of amines and phenols to cyclohexadienone derivative Tetrahedron. 72: 699-705. DOI: 10.1016/J.Tet.2015.12.019 |
0.537 |
|
| 2015 |
Choudhury S, Ahmad S, Khan FA. Effect of bridgehead substitution in the Grob fragmentation of norbornyl ketones: a new route to substituted halophenols. Organic & Biomolecular Chemistry. 13: 9686-96. PMID 26264290 DOI: 10.1039/C5Ob01287B |
0.46 |
|
| 2015 |
Khan FA, Budanur BM, Sudheer C. Bridgehead Substitution via Putative Norborn-1-en-3-ones: Application in the Synthesis of Complex Molecules. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7021-5. PMID 25810279 DOI: 10.1002/Chem.201500131 |
0.467 |
|
| 2015 |
Rao CN, Khan FA. BF3-Et2O mediated skeletal rearrangements of norbornyl appended cyclopentanediols. Organic & Biomolecular Chemistry. 13: 2768-75. PMID 25602974 DOI: 10.1039/C4Ob02423K |
0.462 |
|
| 2015 |
Raveendra Babu K, Khan FA. A domino reaction of tetrahalo-7,7-dimethoxybicyclo[2.2.1]heptenyl alcohols leading to indenones and a de novo synthesis of ninhydrin derivatives. Organic & Biomolecular Chemistry. 13: 299-308. PMID 25367867 DOI: 10.1039/C4Ob01977F |
0.484 |
|
| 2015 |
Rao CN, Khan FA. Triethylamine–Mesyl Chloride/Thionyl Chloride: A Reagent for Hydrodebromination of Diquinane-Based α-Bromo-γ-Lactones Synthesis (Germany). DOI: 10.1055/S-0034-1378843 |
0.407 |
|
| 2015 |
Babu KR, Khan FA. An unusual formation of diarylmethane scaffolds from 4-(halomethyl)cyclohex-2-enone derivatives Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2015.04.128 |
0.464 |
|
| 2015 |
Khan FA, Budanur BM. Superoxide mediated isomerization of 4-aryl-but-1-ynes to 1-aryl-1,3-butadienes Tetrahedron. 71: 7600-7607. DOI: 10.1016/J.Tet.2015.07.075 |
0.48 |
|
| 2015 |
Ahmad S, Choudhury S, Khan FA. Synthesis of marine brominated alkaloid amathamide F: A palladium-catalyzed enamide synthesis Tetrahedron. 71: 4192-4202. DOI: 10.1016/J.Tet.2015.04.091 |
0.414 |
|
| 2015 |
Vasamsetty L, Khan FA, Mehta G. A short, general, Suzuki-Miyaura coupling anchored approach to 3-alkenylbutenolides: Total synthesis of akolactones A & B, hamabiwalactone B and ancepsenolide Tetrahedron. 71: 3209-3215. DOI: 10.1016/J.Tet.2015.04.009 |
0.563 |
|
| 2015 |
Mahadevegowda SH, Khan FA. Diastereoselective synthesis of spirocyclic dihydrofurans and 1-oxaspiro[4.5]decan-6-one derivatives from norbornyl α-diketones European Journal of Organic Chemistry. 2015: 858-870. DOI: 10.1002/Ejoc.201403087 |
0.42 |
|
| 2014 |
Budanur BM, Khan FA. Superoxide chemistry revisited: synthesis of tetrachloro-substituted methylenenortricyclenes. Beilstein Journal of Organic Chemistry. 10: 2531-8. PMID 25383124 DOI: 10.3762/Bjoc.10.264 |
0.47 |
|
| 2014 |
Khan FA, Ahmad S, Kodipelli N, Shivange G, Anindya R. Syntheses of a library of molecules on the marine natural product ianthelliformisamines platform and their biological evaluation. Organic & Biomolecular Chemistry. 12: 3847-65. PMID 24668192 DOI: 10.1039/C3Ob42537A |
0.372 |
|
| 2014 |
Rao GHM, Khan FA. A solvent effect in the reaction of diazomethane with norbornane-2,3-dione 3-hemiketals Synthetic Communications. 44: 3314-3319. DOI: 10.1080/00397911.2014.926554 |
0.402 |
|
| 2014 |
Vasamsetty L, Khan FA, Mehta G. A model approach towards the polycyclic framework present in cembranoid natural products dissectolide A, plumarellide and mandapamate Tetrahedron Letters. 55: 7068-7071. DOI: 10.1016/J.Tetlet.2014.10.141 |
0.503 |
|
| 2014 |
Mahadevegowda SH, Khan FA. Total syntheses of (±)-cis- and (±)-trans-neocnidilides Tetrahedron Letters. 55: 4400-4403. DOI: 10.1016/J.Tetlet.2014.06.007 |
0.339 |
|
| 2014 |
Mahadevegowda SH, Khan FA. Synthesis of the tetrahydrofuran unit of varitriol and γ- butyrolactones from 5-oxabicyclo[2.1.1]hexane derivative via oxidative cleavage reactions Tetrahedron Letters. 55: 2266-2269. DOI: 10.1016/J.Tetlet.2014.02.082 |
0.489 |
|
| 2014 |
Vasamsetty L, Sahu D, Ganguly B, Khan FA, Mehta G. Total synthesis of novel bioactive natural product paracaseolide A and analogues: Computational evaluation of a 'proposed' biomimetic Diels-Alder reaction Tetrahedron. 70: 8488-8497. DOI: 10.1016/J.Tet.2014.09.072 |
0.564 |
|
| 2013 |
Rao GH, Khan FA. An unusual fragmentation of oxetane-embedded tetracyclic ketal systems. The Journal of Organic Chemistry. 78: 11092-5. PMID 24090305 DOI: 10.1021/Jo401870S |
0.463 |
|
| 2013 |
Vasamsetty L, Khan FA, Mehta G. Total synthesis of a novel oxa-bowl natural product paracaseolide A via a 'putative' biomimetic pathway Tetrahedron Letters. 54: 3522-3525. DOI: 10.1016/J.Tetlet.2013.04.097 |
0.532 |
|
| 2013 |
Khan FA, Ahmad S. Synthesis of wilsoniamines A and B Tetrahedron Letters. 54: 2996-2998. DOI: 10.1016/J.Tetlet.2013.03.122 |
0.463 |
|
| 2013 |
Mahadevegowda SH, Khan FA. Grob-type fragmentation of 5-oxabicyclo[2.1.1]hexane system: a strategy for synthesis of annulated and 2,2,5-trisubstituted tetrahydrofurans Tetrahedron. 69: 8494-8504. DOI: 10.1016/J.Tet.2013.07.005 |
0.485 |
|
| 2012 |
Khan FA, Ahmad S. Synthesis of reported and revised structures of amathamide D and synthesis of convolutamine F, H and lutamide A, C. The Journal of Organic Chemistry. 77: 2389-97. PMID 22296242 DOI: 10.1021/Jo3000173 |
0.42 |
|
| 2011 |
Khan FA, Rao CN. Grob Fragmentation of Norbornyl α-Diketones: A Route to α-Ketoenols and Aromatic Compounds Journal of Organic Chemistry. 76: 3320-3328. PMID 21413814 DOI: 10.1021/Jo200223A |
0.376 |
|
| 2011 |
Khan FA, Upadhyay SK. An efficient synthesis of a cyclopentannulated pyrrolidine derivative Synthesis. 2423-2430. DOI: 10.1055/S-0030-1260114 |
0.486 |
|
| 2010 |
Khan FA, Parasuraman K. Synthesis of oxa-bridged derivatives from Diels–Alder bis-adducts of butadiene and 1,2,3,4-tetrahalo-5,5-dimethoxycyclopentadiene Beilstein Journal of Organic Chemistry. 6: 64. PMID 20703377 DOI: 10.3762/Bjoc.6.64 |
0.481 |
|
| 2010 |
Khan FA, Choudhury S. Synthesis and electrochemical properties of substituted para-benzoquinone derivatives Tetrahedron Letters. 51: 2541-2544. DOI: 10.1016/J.Tetlet.2010.03.007 |
0.39 |
|
| 2010 |
Khan FA, Parasuraman K, Donnio B. Synthesis and thermal properties of rigid oxa-bridged-containing dimers and tetramers Tetrahedron. 66: 8745-8755. DOI: 10.1016/J.Tet.2010.09.003 |
0.358 |
|
| 2010 |
Khan FA, Choudhury S. An Efficient Synthesis of Substituted meta-Halophenols and Their Methyl Ethers: Insight into the Reaction Mechanism European Journal of Organic Chemistry. 2010: 2954-2970. DOI: 10.1002/Ejoc.201000071 |
0.506 |
|
| 2009 |
Khan FA, Sudheer C. An efficient method for zinc mediated reduction of norbornyl α-diketones in [bmim][BF4]:H2O Arkivoc. 2009: 222-228. DOI: 10.3998/Ark.5550190.0010.721 |
0.374 |
|
| 2009 |
Khan FA, Upadhyay SK. Synthesis and electrochemical signature of novel norbornyl-ferrocene hybrids Synthesis. 2773-2777. DOI: 10.1055/S-0029-1217601 |
0.457 |
|
| 2009 |
Khan FA, Rao CN. Synthesis of 9-oxa-noradamantane derivative, an aesthetically pleasing 'oxa-basket' Tetrahedron Letters. 50: 5751-5753. DOI: 10.1016/J.Tetlet.2009.07.143 |
0.494 |
|
| 2009 |
Khan FA, Sudheer C. Oxygen as moderator in the zinc-mediated reduction of aromatic nitro to azoxy compounds Tetrahedron Letters. 50: 3394-3396. DOI: 10.1016/J.Tetlet.2009.02.122 |
0.362 |
|
| 2009 |
Khan FA, Sudheer C. Ruthenium‐Mediated Oxidation under Buffered Conditions: A Simple and Useful Protocol for the Synthesis of Norbornyl α‐Diketones with Acid Sensitive Functionalities Advanced Synthesis & Catalysis. 351: 939-944. DOI: 10.1002/Adsc.200900042 |
0.397 |
|
| 2008 |
Khan FA, Sudheer C. A chiral pool approach to the synthesis of optically active tetrahalo norbornyl building blocks. Organic Letters. 10: 3029-3032. PMID 18549232 DOI: 10.1021/Ol800990M |
0.402 |
|
| 2008 |
Khan FA, Upadhyay SK. A stereoselective C7nC5x free-radical cascade route to optically pure and potentially useful tetracyclic amines Tetrahedron Letters. 49: 6111-6114. DOI: 10.1016/J.Tetlet.2008.08.013 |
0.399 |
|
| 2007 |
Khan FA, Sudheer C, Soma L. Lead(IV) acetate: intriguing reactivity profile Chemical Communications. 4239-41. PMID 18217592 DOI: 10.1039/B708268A |
0.392 |
|
| 2007 |
Khan FA, Rout B. A formal total synthesis of (±)-neplanocin A Journal of Organic Chemistry. 72: 7011-7013. PMID 17665958 DOI: 10.1021/Jo0710127 |
0.347 |
|
| 2007 |
Khan FA, Rao GHM, Satapathy R, Parasuraman K. Serendipitously discovered diazomethane-mediated novel molecular rearrangements of norbornyl alpha-ketohemiketals. Organic Letters. 9: 1581-1584. PMID 17373805 DOI: 10.1021/Ol070442G |
0.41 |
|
| 2007 |
Khan FA, Krishnakumar KS, Sudheer C. Synthesis of Highly Functionalized δ-Lactone-Fused Cyclopentanoids Synthesis. 2007: 1054-1060. DOI: 10.1055/S-2007-965948 |
0.429 |
|
| 2007 |
Khan FA, Dwivedi V, Rout B. Synthesis of a novel, bowl-like bis γ-lactone Tetrahedron Letters. 48: 207-209. DOI: 10.1016/J.Tetlet.2006.11.062 |
0.493 |
|
| 2007 |
Khan FA, Soma L. Synthesis of tribromobenzofuran and tribromobenzopyran derivatives from methyl 2-allyl-4,5,6-tribromo-3-hydroxybenzoate Tetrahedron Letters. 48: 85-88. DOI: 10.1016/J.Tetlet.2006.11.005 |
0.414 |
|
| 2006 |
Khan FA, Choudhury S. Synthesis of Trichlorophenol Derivatives Synthetic Communications. 36: 3749-3760. DOI: 10.1080/00397910600946330 |
0.45 |
|
| 2006 |
Khan FA, Rao CN. An efficient synthesis of diquinane-based bis-γ-lactones Tetrahedron Letters. 47: 7567-7570. DOI: 10.1016/J.Tetlet.2006.08.092 |
0.503 |
|
| 2006 |
Khan FA, Rout B. Total synthesis of (±)-pentenomycin Tetrahedron Letters. 47: 5251-5253. DOI: 10.1016/J.Tetlet.2006.05.156 |
0.336 |
|
| 2006 |
Reißig H, Khan FA, Czerwonka R, Dinesh CU, Shaikh AL, Zimmer R. Benzannulated Cyclooctanol Derivatives by Samarium Diiodide Induced Intramolecular Carbonyl–Alkene Coupling – Scope, Limitations, Stereoselectivity European Journal of Organic Chemistry. 2006: 4419-4428. DOI: 10.1002/Ejoc.200600360 |
0.688 |
|
| 2006 |
Khan FA, Choudhury S. An Efficient Route to Pentasubstituted Phenols European Journal of Organic Chemistry. 2006: 672-676. DOI: 10.1002/Ejoc.200500603 |
0.398 |
|
| 2005 |
Khan FA, Dash J, Sudheer Ch, Sahu N, Parasuraman K. Concise synthesis of novel oxa-bridged compounds. The Journal of Organic Chemistry. 70: 7565-77. PMID 16149785 DOI: 10.1021/Jo0507385 |
0.74 |
|
| 2005 |
Khan FA, Sudheer C, Sahu N. 1‐Butyl‐3‐methyl‐imidazolium Tetrafluoroborate as a Recyclable Reaction Medium for Henry Reaction Synthetic Communications. 35: 201-207. DOI: 10.1081/Scc-200048415 |
0.364 |
|
| 2005 |
Khan FA, Satapathy R, Sudheer C, Rao CN. A new reaction of diazomethane with norbornyl α-diketones Tetrahedron Letters. 46: 7193-7196. DOI: 10.1016/J.Tetlet.2005.08.087 |
0.358 |
|
| 2005 |
Khan FA, Sahu N. Highly efficient and recyclable ruthenium-based supported catalysts Journal of Catalysis. 231: 438-442. DOI: 10.1016/J.Jcat.2005.02.001 |
0.315 |
|
| 2004 |
Khan FA, Satapathy R, Dash J, Savitha G. A rapid and stereoselective route to the trans-hydrindane ring system. The Journal of Organic Chemistry. 69: 5295-301. PMID 15287773 DOI: 10.1021/Jo049615V |
0.739 |
|
| 2004 |
Khan FA, Dash J, Sudheer Ch. Indium-mediated regio- and diastereoselective reduction of norbornyl alpha-diketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 2507-19. PMID 15146523 DOI: 10.1002/Chem.200305656 |
0.734 |
|
| 2004 |
Khan FA, Dash J, Rout B. A short and stereoselective synthesis of functionalized pentenomycin derivatives Tetrahedron Letters. 45: 9285-9288. DOI: 10.1016/J.Tetlet.2004.10.065 |
0.752 |
|
| 2004 |
Khan FA, Dash J, Satapathy R, Upadhyay SK. Hydrotalcite catalysis in ionic liquid medium: a recyclable reaction system for heterogeneous Knoevenagel and nitroaldol condensation Tetrahedron Letters. 45: 3055-3058. DOI: 10.1016/J.Tetlet.2004.02.103 |
0.693 |
|
| 2004 |
Khan F, Dash J. Diastereoselection During Allylindium Addition to Norbornylα-Diketones European Journal of Organic Chemistry. 2004: 2692-2700. DOI: 10.1002/Ejoc.200400044 |
0.72 |
|
| 2003 |
Khan FA, Dash J. A novel and expeditious approach to unusual spirolactam building blocks. The Journal of Organic Chemistry. 68: 4556-9. PMID 12762770 DOI: 10.1021/Jo034023I |
0.737 |
|
| 2003 |
Khan FA, Dash J, Sudheer C, Gupta RK. Chemoselective reduction of aromatic nitro and azo compounds in ionic liquids using zinc and ammonium salts Tetrahedron Letters. 44: 7783-7787. DOI: 10.1016/J.Tetlet.2003.08.080 |
0.708 |
|
| 2002 |
Khan FA, Dash J, Sahu N, Sudheer Ch. An easy access to gamma-lactone-fused cyclopentanoids. The Journal of Organic Chemistry. 67: 3783-7. PMID 12027694 DOI: 10.1021/Jo025521E |
0.703 |
|
| 2002 |
Khan FA, Dash J, Sahu N, Gupta S. Regio- and diastereoselective reduction of nonenolizable alpha-diketones to acyloins mediated by indium metal. Organic Letters. 4: 1015-8. PMID 11893210 DOI: 10.1021/Ol025593S |
0.719 |
|
| 2002 |
Khan FA, Dash J. Synthesis of a novel, highly symmetric bis-oxa-bridged compound. Journal of the American Chemical Society. 124: 2424-5. PMID 11890776 DOI: 10.1021/Ja017371F |
0.736 |
|
| 2001 |
Khan FA, Dash J, Jain D, Prabhudas B. Rearrangement of 1,4,5,6-tetrahalo-7,7-dimethoxybicyclo[2.2.1]hept-5-en-2-ones to phenolic derivatives Journal of the Chemical Society-Perkin Transactions 1. 3132-3134. DOI: 10.1039/B108152G |
0.361 |
|
| 2000 |
Zimmer R, Dinesh CU, Nandanan E, Khan FA. Palladium-catalyzed reactions of allenes. Chemical Reviews. 100: 3067-3126. PMID 11749314 DOI: 10.1021/Cr9902796 |
0.395 |
|
| 2000 |
Khan FA, Prabhudas B, Dash aJ, Sahu N. A Ruthenium-Catalyzed, Novel and Facile Procedure for the Conversion of Vicinal Dihaloalkenes to α-Diketones Journal of the American Chemical Society. 122: 9558-9559. DOI: 10.1021/Ja001956C |
0.378 |
|
| 2000 |
Khan FA, Prabhudas B. Indium-Mediated, Highly Efficient and Diastereoselective Addition of Cyclic Secondary Allylic Bromides to Carbonyl Compounds Tetrahedron. 56: 7595-7599. DOI: 10.1016/S0040-4020(00)00672-4 |
0.466 |
|
| 2000 |
Khan FA, Prabhudas B, Dash J. 1,2,3,4-Tetrachloro-5,5-dimethoxy-cyclopenta-1,3-diene: Diels Alder Reactions and Applications of the Products Formed Journal Fur Praktische Chemie-Chemiker-Zeitung. 342: 512-517. DOI: 10.1002/1521-3897(200006)342:5<512::Aid-Prac512>3.0.Co;2-V |
0.745 |
|
| 2000 |
Khan FA, Czerwonka R, Reissig H. Pd‐Catalyzed Reactions of Donor−Acceptor‐Substituted Cyclopropanes and Their Ring‐Opened Derivatives: Attempted Heck Cyclization and Novel One‐Pot Enolate Arylations European Journal of Organic Chemistry. 2000: 3607-3617. DOI: 10.1002/1099-0690(200011)2000:21<3607::Aid-Ejoc3607>3.0.Co;2-N |
0.669 |
|
| 1999 |
Zimmer R, Zahn G, Khan FA, Reissig H-. Configurational analysis of 14,14-dimethyl-12-oxatricyclo[9.2.1.03,8]tetradeca-3,5,7-trien-13-one Acta Crystallographica Section C-Crystal Structure Communications. 55: 1941-1943. DOI: 10.1107/S0108270199009014 |
0.593 |
|
| 1999 |
Khan FA, Prabhudas B. A simple and preparatively useful tributylstannane mediated selective reduction and bridgehead functionalization of tetrahalonorbornene derivatives Tetrahedron Letters. 40: 9289-9292. DOI: 10.1016/S0040-4039(99)01948-6 |
0.396 |
|
| 1997 |
Khan FA, Czerwonka R, Zimmer R, Reissig H. A Novel Sm(II)-Induced Route to Highly Substituted Benzannulated Cyclooctanol Derivatives Synlett. 1997: 995-997. DOI: 10.1055/S-1997-934 |
0.671 |
|
| 1997 |
Khan FA, Zimmer R. Samarium Diiodide: A Mild and Selective Reagent in organic synthesis Journal Fur Praktische Chemie-Chemiker-Zeitung. 339: 101-104. DOI: 10.1002/Prac.19973390120 |
0.369 |
|
| 1996 |
Khan FA, Czerwonka R, Reissig H. A Novel Pd(0)-Catalyzed One-Pot Transformation Of Substituted Siloxycyclopropanes To Indane Derivatives Synlett. 1996: 533-535. DOI: 10.1055/S-1996-5483 |
0.583 |
|
| 1996 |
Mehta G, Khan FA, Mohal N, Namboothiri INN, Kalyanaraman P, Chandrasekhar J. π-Face selectivities in nucleophilic additions to 2-endo-arylnorbornan-7-ones: the role of through-space electrostatic interactions Journal of the Chemical Society-Perkin Transactions 1. 2665-2667. DOI: 10.1039/P19960002665 |
0.49 |
|
| 1996 |
Zimmer R, Khan FA. Methoxyallene: A Reagent of Versatile Applications in organic synthesis Journal Fur Praktische Chemie-Chemiker-Zeitung. 338: 92-94. DOI: 10.1002/Prac.19963380116 |
0.337 |
|
| 1994 |
Mehta G, Khan FA, Ganguly B, Chandrasekhar J. π-Facial diastereoselection in reductions of sterically unbiased ketones containing the norbornyl framework: further tests for theoretical models Journal of the Chemical Society-Perkin Transactions 1. 2275-2277. DOI: 10.1039/P29940002275 |
0.459 |
|
| 1994 |
Mehta G, Khan FA, Gadre SR, Shirsat RN, Ganguly B, Chandrasekhar J. Electrostatic vs. Orbital Control of Facial Selectivities in ? Systems: Experimental and Theoretical Study of Electrophilic Additions to 7-Isopropylidenenorbornanes Angewandte Chemie International Edition in English. 33: 1390-1392. DOI: 10.1002/Anie.199413901 |
0.428 |
|
| 1994 |
Mehta G, Khan FA, Gadre SR, Shirsat RN, Ganguly B, Chandrasekhar J. Elektrostatisch oder Orbital-kontrollierte Seitendifferenzierung von π-Elektronensystemen: experimentelle und theoretische Untersuchung elektrophiler Additionen an 7-Isopropylidennorbonane Angewandte Chemie. 106: 1433-1435. DOI: 10.1002/Ange.19941061317 |
0.387 |
|
| 1993 |
Mehta G, Khan FA. Short, Convenient Preparative Procedures for 7-Isopropylidenenorbornane, 7-Isopropylidenenorbornene, and 7-Isopropylidenenorbornadiene Synthetic Communications. 23: 2985-2990. DOI: 10.1080/00397919308011141 |
0.525 |
|
| 1993 |
Mehta G, Khan FA. Long-range substituent effects on the regioselectivity of one-carbon ring expansion of norbornan-7-ones Journal of the Chemical Society-Perkin Transactions 1. 1727-1728. DOI: 10.1039/P19930001727 |
0.511 |
|
| 1993 |
Ganguly B, Chandrasekhar J, Khan FA, Mehta G. A simple computational model for predicting .pi.-facial selectivity in reductions of sterically unbiased ketones. Relative importance of electrostatic and orbital interactions Journal of Organic Chemistry. 58: 1734-1739. DOI: 10.1021/Jo00059A022 |
0.453 |
|
| 1992 |
Mehta G, Khan FA, Ganguly B, Chandrasekhar J. Importance of orbital and electrostatic interactions in determining π-facial selectivities in nucleophilic additions to endo-substituted bicyclo[2.2.2]octan-2-ones Journal of the Chemical Society, Chemical Communications. 1711-1712. DOI: 10.1039/C39920001711 |
0.494 |
|
| 1992 |
Kumar VA, Venkatesan K, Ganguly B, Chandrasekhar J, Khan FA, Mehta G. Ground state geometric distortions image distal substituent effects in determining the β-facial selectivity in 7-norbornenones Tetrahedron Letters. 33: 3069-3072. DOI: 10.1016/S0040-4039(00)79602-X |
0.449 |
|
| 1992 |
Mehta G, Khan FA. Modulation of π-facial selectivities in nucleophilic additions to 7-norbornenones Tetrahedron Letters. 33: 3065-3068. DOI: 10.1016/S0040-4039(00)79601-8 |
0.473 |
|
| 1992 |
Mehta G, Khan FA, Lakshmi KA. Modification of π-face selectivity of 7-norbornenones during reduction in β-cyclodextrin and solid state Tetrahedron Letters. 33: 7977-7980. DOI: 10.1016/S0040-4039(00)74793-9 |
0.457 |
|
| 1991 |
Mehta G, Khan FA. Electronic control of π-facial diastereoselection. Electrophilic additions to 7-methylenenorbornanes Journal of the Chemical Society, Chemical Communications. 18-19. DOI: 10.1039/C39910000018 |
0.437 |
|
| 1990 |
Mehta G, Khan FA. Electronic control of .pi.-facial selectivities in nucleophilic additions to 7-norbornanones Journal of the American Chemical Society. 112: 6140-6142. DOI: 10.1021/Ja00172A047 |
0.425 |
|
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