| Year |
Citation |
Score |
| 2020 |
Yadav VK, Prasad DLVK, Yadav A, Yadav K. On the solvent‐ and temperature‐driven stereoselectivity of the Diels–Alder cycloaddition reactions of furan with maleic anhydride and maleimide Journal of Physical Organic Chemistry. DOI: 10.1002/Poc.4131 |
0.385 |
|
| 2014 |
Yadav VK, Verma AK, Kumar P, Hulikal V. 2-Arylcyclopropylmethanol as a substitute for homoallyl aryl alcohol in the construction of cis-2,6-disubstituted tetrahydropyran: synthesis of (±)-centrolobine. Chemical Communications (Cambridge, England). 50: 15457-60. PMID 25354489 DOI: 10.1039/C4Cc07796B |
0.392 |
|
| 2014 |
Yadav VK, Naganaboina VK, Hulikal V. Allylsilane-interrupted homo-Nazarov cyclization and synthesis of bicyclo[3.2.1]octan-8-ones Tetrahedron Letters. 55: 2015-2018. DOI: 10.1016/J.Tetlet.2014.02.018 |
0.466 |
|
| 2014 |
Yadav VK, Naganaboina VK, Hulikal V. ChemInform Abstract: Allylsilane-Interrupted Homo-Nazarov Cyclization and Synthesis of Bicyclo[3.2.1]octan-8-ones. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201435193 |
0.349 |
|
| 2013 |
Yadav VK, Narhe BD, Kumar K, Hulikal V. A Route to 2-Alkenyl-3-(tert-butyldiphenylsilyl)amines and Application to the Construction of a Tricyclic Ring System European Journal of Organic Chemistry. 2013: 4163-4174. DOI: 10.1002/Ejoc.201300319 |
0.375 |
|
| 2012 |
Narhe BD, Sriramurthy V, Yadav VK. A smooth rearrangement of N-p-toluenesulfonyl 2-tert-butyldiphenylsilylmethyl-substituted azetidines into N-p-toluenesulfonyl 3-tert-butyldiphenylsilyl-substituted pyrrolidines. Organic & Biomolecular Chemistry. 10: 4390-9. PMID 22562598 DOI: 10.1039/C2Ob07140A |
0.355 |
|
| 2010 |
YADAV VK, KAPOOR KK. ChemInform Abstract: 3,4-Dehydro-2-hydroxy-6-(2-phenethyl)tetrahydropyran. 1,3-Acyclic Diastereoselection in Reaction with MeOH and Its Application in the Synthesis of a Racemic Mevinolin Analogue. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199615274 |
0.34 |
|
| 2010 |
YADAV V, FALLIS AG. ChemInform Abstract: Free-Radical Based Cycloalkanol Synthesis and Annulation from Thioacetal Precursors. Cheminform. 22: no-no. DOI: 10.1002/chin.199139081 |
0.567 |
|
| 2009 |
Agrawal D, Sriramurthy V, Yadav VK. Corrigendum to “4,5-Didehydro-7-silyloxymethyl-2-oxepanone and formal total syntheses of Hagen’s gland lactones and trans-kumausynes” [Tetrahedron Lett. 47 (2006) 7615] Tetrahedron Letters. 50: 2026. DOI: 10.1016/J.Tetlet.2009.02.096 |
0.347 |
|
| 2009 |
Yadav VK, Gupta A. ChemInform Abstract: Reaction of 2-Silylmethylcyclopropyl Ketones with in situ Oxirane-Derived Aldehydes and Formation of 2-Hydroxymethyl Tetrahydrofurans. Cheminform. 40. DOI: 10.1002/CHIN.200947080 |
0.312 |
|
| 2008 |
Yadav VK, Kumar NV. 2,3-Heteroaromatic ring-fused cyclohexanones via heteroaromatic homo-Nazarov cyclization of donor-acceptor substituted cyclopropanes. Chemical Communications (Cambridge, England). 3774-6. PMID 18685773 DOI: 10.1039/b805348k |
0.321 |
|
| 2008 |
Yadav VK, Gupta A. A new synthesis of pyrrolidines via imino-aldol reaction of (2-trimethylsilylmethyl)cyclopropyl ketones with imines Tetrahedron Letters. 49: 3212-3215. DOI: 10.1016/J.Tetlet.2008.03.117 |
0.475 |
|
| 2008 |
Yadav VK, Gupta A. ChemInform Abstract: A New Synthesis of Pyrrolidines via Imino-Aldol Reaction of (2-Trimethylsilylmethyl)cyclopropyl Ketones with Imines. Cheminform. 39. DOI: 10.1002/CHIN.200835059 |
0.331 |
|
| 2007 |
Yadav VK, Kumar NV, Parvez M. Lewis acid-catalyzed formation of indene derivatives via tandem reactions of arylacetylenes with the cations generated from 2-silylmethyl cyclopropyl carbinols. Chemical Communications (Cambridge, England). 2281-3. PMID 17534517 DOI: 10.1039/b700246g |
0.318 |
|
| 2007 |
Gupta A, Yadav VK. A Highly Diastereoselective Approach to Tetrahydrofurans via [3 + 2] Cycloadditions of Silylmethyl-Substituted Cyclopropanes with Aldehydes and Ketones. Cheminform. 38. DOI: 10.1002/CHIN.200708109 |
0.327 |
|
| 2006 |
Yadav VK, Gupta A, Balamurugan R, Sriramurthy V, Kumar NV. Distinguishing the early and late transition states and exploring the validity of sigma --> sigma*#, sigma# --> sigma*, and sigma --> pi*(C=O) concepts in diastereoselection from NBO analysis. The Journal of Organic Chemistry. 71: 4178-82. PMID 16709058 DOI: 10.1021/Jo060291F |
0.645 |
|
| 2006 |
Gupta A, Yadav VK. Corrigendum to “A highly diastereoselective approach to tetrahydrofurans via [3+2] cycloadditions of silylmethyl-substituted cyclopropanes with aldehydes and ketones” Tetrahedron Letters. 47: 9159. DOI: 10.1016/J.Tetlet.2006.10.091 |
0.413 |
|
| 2006 |
Gupta A, Yadav VK. A highly diastereoselective approach to tetrahydrofurans via [3+2] cycloadditions of silylmethyl-substituted cyclopropanes with aldehydes and ketones Tetrahedron Letters. 47: 8043-8047. DOI: 10.1016/J.TETLET.2006.09.064 |
0.327 |
|
| 2006 |
Agrawal D, Sriramurthy V, Yadav VK. 4,5-Didehydro-7-silyloxymethyl-2-oxepanone and formal total syntheses of Hagen’s gland lactones and trans-kumausynes Tetrahedron Letters. 47: 7615-7618. DOI: 10.1016/J.Tetlet.2006.08.059 |
0.395 |
|
| 2005 |
Yadav VK, Sriramurthy V. Silylmethyl-substituted aziridine and azetidine as masked 1,3- and 1,4-dipoles for formal [3 + 2] and [4 + 2] cycloaddition reactions. Journal of the American Chemical Society. 127: 16366-7. PMID 16305202 DOI: 10.1021/Ja055664T |
0.445 |
|
| 2004 |
Yadav VK, Sriramurthy V. Formal [3+2] addition of acceptor-substituted cyclopropylmethylsilanes with aryl acetylenes. Angewandte Chemie (International Ed. in English). 43: 2669-71. PMID 18629985 |
0.35 |
|
| 2004 |
Yadav VK, Sriramurthy V. Formal [3 + 2] and [3 + 3] additions of acceptor-substituted cyclopropylmethylsilanes to allenylsilanes. Organic Letters. 6: 4495-8. PMID 15548059 DOI: 10.1021/Ol047991W |
0.427 |
|
| 2004 |
Yadav VK, Senthil G, Singh L, Parvez M. On the reaction of 1-oxa-4-thiaspiro[4.5]decan-7-one with PhLi. A reinvestigation. The Journal of Organic Chemistry. 69: 8131-2. PMID 15527305 DOI: 10.1021/Jo0489364 |
0.341 |
|
| 2004 |
Yadav VK, Kumar NV. Highly stereoselective prins cyclization of silylmethyl-substituted cyclopropyl carbinols to 2,4,6-trisubstituted tetrahydropyrans. Journal of the American Chemical Society. 126: 8652-3. PMID 15250708 DOI: 10.1021/Ja048000C |
0.458 |
|
| 2003 |
Nishizawa M, Takao H, Yadav VK, Imagawa H, Sugihara T. Mercuric triflate-(TMU)3-catalyzed cyclization of omega-arylalkyne leading to dihydronaphthalenes. Organic Letters. 5: 4563-5. PMID 14627384 DOI: 10.1021/Ol035622E |
0.384 |
|
| 2003 |
Yadav VK, Balamurugan R. Diastereoselective aldol reactions of enolates generated from vicinally substituted trimethylsilylmethyl cyclopropyl ketones. Organic Letters. 5: 4281-4. PMID 14601980 DOI: 10.1021/Ol035481G |
0.684 |
|
| 2003 |
Yadav VK, Babu K, Balamurugan R. Bicyclo[2.1.1]hexan-2-one as a new probe for the study of π-facial selectivity in nucleophilic additions. A comment Tetrahedron Letters. 44: 6617-6619. DOI: 10.1016/S0040-4039(03)01681-2 |
0.635 |
|
| 2002 |
Yadav VK, Balamurugan R. Synthesis of gamma-methylene oxacycles and alpha- and beta-alkylidene lactones via silicon-assisted ring opening of cyclopropyl carbinols. Chemical Communications (Cambridge, England). 514-5. PMID 12120567 DOI: 10.1039/B111332C |
0.642 |
|
| 2002 |
Yadav VK, Senthil G, Babu KG, Parvez M, Reid JL. Heteroatom influence on the pi-facial selectivity of Diels-Alder cycloadditions to 1-oxa-4-thia-6-vinylspiro[4.5]dec-6-ene, 3-methoxy-3-methyl-2-vinylcyclohexene, and 3-methoxy-2-vinylcyclohexene. The Journal of Organic Chemistry. 67: 1109-17. PMID 11846651 DOI: 10.1021/Jo0106400 |
0.325 |
|
| 2002 |
Yadav VK, Balamurugan R. 4-Oxatricyclo[5.2.1.0(2,6)]decan-10-one and 4-oxatricyclo[5.2.1.0(2,6)]dec-8-en-10-one. Experimental and DFT investigations of the pi-selectivities. The Journal of Organic Chemistry. 67: 587-90. PMID 11798335 DOI: 10.1021/Jo015945T |
0.641 |
|
| 2001 |
Parvez M, Yadav VK, Balamurugan R. pi-Facial selectivities of diastereotopic ketones: p-bromobenzoates of 4-hetero-1-decalinols. Acta Crystallographica. Section C, Crystal Structure Communications. 57: 1084-8. PMID 11588379 DOI: 10.1107/S0108270101009544 |
0.659 |
|
| 2001 |
Yadav VK, Balamurugan R. Silicon-assisted ring opening of donor-acceptor substituted cyclopropanes. An expedient entry to substituted dihydrofurans. Organic Letters. 3: 2717-9. PMID 11506617 DOI: 10.1021/Ol0163169 |
0.693 |
|
| 2001 |
Parvez M, Senthil G, Yadav VK. 7-Phenyl-1-oxa-4-thiaspiro[4.5]decan-7-ol stereoisomers. Acta Crystallographica Section C-Crystal Structure Communications. 57: 577-579. PMID 11353257 DOI: 10.1107/S0108270101001573 |
0.328 |
|
| 2001 |
Parvez M, Yadav VK, Senthil G. Some Diels-Alder adducts of 6-vinyl-1-oxa-4-thiaspiro[4.5]dec-6-ene. Acta Crystallographica Section C-Crystal Structure Communications. 57: 82-85. PMID 11173407 DOI: 10.1107/S0108270100013597 |
0.332 |
|
| 2001 |
Parvez M, Yadav VK, Senthil G. Johnson orthoester Claisen rearrangement products of some (1-oxa-4-thiaspiro[4.5]dec-6-en-6-yl)alkanols Acta Crystallographica Section C-Crystal Structure Communications. 57: 79-81. PMID 11173406 DOI: 10.1107/S0108270100013603 |
0.336 |
|
| 2001 |
Yadav VK, Sriramurthy V. A detailed ab initio MO investigation of the diastereoselectivities of five- and six-membered ring ketones bearing O and S, C and S, and C and O substituents at the α-carbon Tetrahedron. 57: 3987-3995. DOI: 10.1016/S0040-4020(01)00276-9 |
0.402 |
|
| 2000 |
Yadav VK, Williams P, Benn M. The synthesis of hydroxysmirnovine Canadian Journal of Chemistry. 78: 542-545. DOI: 10.1139/V00-053 |
0.6 |
|
| 2000 |
Yadav VK, Jeyaraj DA, Parvez M. The suitability of anion-accelerated oxy-Cope rearrangement as a probe to study π-facial selectivity. An experimental study with (6-methyl-1-oxa-4-thiaspiro[4.5]dec-6-en-7-yl)(allyl)methanols Journal of the Chemical Society-Perkin Transactions 1. 1423-1428. DOI: 10.1039/A909839I |
0.395 |
|
| 2000 |
Yadav VK, Jeyaraj DA, Balamurugan R. The Cation Complexation Model Predicts the Experimental π-Facial Selectivity of 2-ax- and 2-eq-Substituted Cyclohexanones. A Detailed Ab Initio MO Investigation Tetrahedron. 56: 7581-7589. DOI: 10.1016/S0040-4020(00)00663-3 |
0.644 |
|
| 2000 |
Yadav VK, Williams P, Benn M. ChemInform Abstract: The Synthesis of Hydroxysmirnovine. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200042210 |
0.587 |
|
| 1999 |
Yadav VK, Jeyaraj DA, Parvez M, Yamdagni R. 7-Hydroxymethyl-6-methyl-1-oxa-4-thiaspiro[4.5]dec-6-ene. Exceptionally High Anti to Sulfur Diastereoselectivity under Conditions of Johnson Ortho Ester Claisen Rearrangement Favors Cieplak Mode of Diastereoselection. The Journal of Organic Chemistry. 64: 2928-2932. PMID 11674369 DOI: 10.1021/Jo981634F |
0.311 |
|
| 1999 |
Yadav VK, Senthil G, Jeyaraj DA. Diastereofacial selectivities of substituted 5-aza- and 5-bora-2-adamantanones. Application of the complexation model and its ab initio MO investigation Tetrahedron. 55: 14211-14218. DOI: 10.1016/S0040-4020(99)00888-1 |
0.348 |
|
| 1998 |
Yadav VK, Jeyaraj DA. 4-Substituted Cyclohexanones. Predicting the Facial Selectivity of Nucleophilic Attacks from the Geometrical Changes on Cation−Carbonyl Complexation: An ab Initio Investigation The Journal of Organic Chemistry. 63: 3474-3477. DOI: 10.1021/Jo972006L |
0.387 |
|
| 1998 |
Jeyaraj DA, Yadav VK, Parvez M, Gauniyal HM. An Investigation of the Diastereoselectivity of Nucleophilic Additions to 6-Methyl-1-oxa-4-thiaspiro[4.5]dec-6-ene-7-carbaldehyde. Hybridization of the Nucleophile Alters the Diastereoselectivity† The Journal of Organic Chemistry. 63: 3831-3837. DOI: 10.1021/Jo971697I |
0.391 |
|
| 1998 |
Jeyaraj DA, Kapoor KK, Yadav VK, Gauniyal HM, Parvez M. DBU-Catalyzed Deconjugation of 7-Substituted 3,4-Didehydro-2-oxepanones. Deuterium Incorporation, Significance of the Imine Double Bond, and Application to the Synthesis of a Key Pharmacophore The Journal of Organic Chemistry. 63: 287-294. DOI: 10.1021/Jo971417Z |
0.431 |
|
| 1997 |
Parvez M, Jeyaraj DA, Yadav VK. Oxa-thia-spiro-decene Derivatives Acta Crystallographica Section C Crystal Structure Communications. 53: 1961-1963. DOI: 10.1107/S0108270197009591 |
0.346 |
|
| 1997 |
Jeyaraj DA, Yadav VK. 3-Halocyclohexanones. Torsion angle changes after cation-carbonyl complexation dictate the facial selectivity in reactions with nucleophiles: An ab initio investigation Tetrahedron Letters. 38: 6095-6098. DOI: 10.1016/S0040-4039(97)01376-2 |
0.321 |
|
| 1997 |
Jeyaraj DA, Yadav A, Yadav VK. The directional changes in torsion angles alone after complexation of the carbonyl oxygen with a prototypical cation such as H+ predict the facial selectivity of substituted cyclohexanones. An ab initio investigation Tetrahedron Letters. 38: 4483-4486. DOI: 10.1016/S0040-4039(97)00910-6 |
0.325 |
|
| 1994 |
Yadav VK, Kapoor KK. Al2O3 supported KF: An efficient mediator in the epoxidation of electron deficient alkenes with t-BuOOH Tetrahedron Letters. 35: 9481-9484. DOI: 10.1016/S0040-4039(00)78577-7 |
0.305 |
|
| 1991 |
Yadav V, Fallis AG. Free-radical based cycloalkanol synthesis and annulation from thioacetal precursors Canadian Journal of Chemistry. 69: 779-789. DOI: 10.1139/V91-116 |
0.626 |
|
| 1990 |
YADAV V, FALLIS AG. ChemInform Abstract: Cyclopentane Synthesis and Annulation. Part 2. Radical Cyclizations of Oxathiolanones. Cheminform. 21. DOI: 10.1002/chin.199007112 |
0.598 |
|
| 1989 |
Yadav V, G. Fallis A. Cyclopentane synthesis and annulation II: Radical cyclizations of oxathiolanones Tetrahedron Letters. 30: 3283-3286. DOI: 10.1016/S0040-4039(00)99222-0 |
0.33 |
|
| 1988 |
Yadav VK, Fallis AG. Cyclopentane synthesis and annulation: Intramolecular radical cyclization of acetals Tetrahedron Letters. 29: 897-900. DOI: 10.1016/S0040-4039(00)82476-4 |
0.636 |
|
| 1988 |
YADAV VK, FALLIS AG. ChemInform Abstract: Cyclopentane Synthesis and Annulation: Intramolecular Radical Cyclization of Acetals. Cheminform. 19. DOI: 10.1002/chin.198830092 |
0.613 |
|
| 1987 |
YADAV VK, FALLIS AG. ChemInform Abstract: Regioselective Cleavage of 2-Methyltetrahydrofuran: A Versatile Synthesis of 1-Halo-4-pentanols and 4-Halo-1-pentanols. Cheminform. 18. DOI: 10.1002/chin.198708106 |
0.583 |
|
| 1986 |
Yadav VK, Fallis AG. Regioselective cleavage of 2-methyltetrahydrofuran: a versatile synthesis of 1-halo-4-pentanols and 4-halo-1-pantanols The Journal of Organic Chemistry. 51: 3372-3374. DOI: 10.1021/Jo00367A025 |
0.593 |
|
| 1986 |
ATTAH-POKU SK, CHAU F, YADAV VK, FALLIS AG. ChemInform Abstract: Intramolecular Routes to Hydrindanes: The Diels-Alder and Michael-Aldol Approach to 6-Isopropyl-9-methylbicyclo[4.3.0]nonan-3-one. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198602176 |
0.556 |
|
| 1985 |
Attah-Poku SK, Chau F, Yadav VK, Fallis AG. Intramolecular routes to hydrindanes: the Diels-Alder and Michael aldol approach to 6-isopropyl-9-methylbicyclo[4.3.0]nonan-3-one The Journal of Organic Chemistry. 50: 3418-3419. DOI: 10.1002/Chin.198602176 |
0.58 |
|
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