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Veejendra K. Yadav

Department of Chemistry

Indian Institute of Technology

Kanpur 208 016

India

[email]@iitk.ac.in

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Chemistry, Indian Institute of Technology, Kanpur 208 016, India. 2001 - 2012

References

  1. A smooth rearrangement of N-p-toluenesulfonyl 2-tert-butyldiphenylsilylmethyl-substituted azetidines into N-p-toluenesulfonyl 3-tert-butyldiphenylsilyl-substituted pyrrolidines. Narhe, B.D., Sriramurthy, V., Yadav, V.K. Org. Biomol. Chem. (2012) [Pubmed]
  2. 2,3-Heteroaromatic ring-fused cyclohexanones via heteroaromatic homo-Nazarov cyclization of donor-acceptor substituted cyclopropanes. Yadav, V.K., Kumar, N.V. Chem. Commun. (Camb.) (2008) [Pubmed]
  3. Lewis acid-catalyzed formation of indene derivatives via tandem reactions of arylacetylenes with the cations generated from 2-silylmethyl cyclopropyl carbinols. Yadav, V.K., Kumar, N.V., Parvez, M. Chem. Commun. (Camb.) (2007) [Pubmed]
  4. Total syntheses of (+)-7-epi-goniofufurone, (+)-goniopypyrone and (+)-goniofufurone from a common precursor. Yadav, V.K., Agrawal, D. Chem. Commun. (Camb.) (2007) [Pubmed]
  5. 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. Yadav, V.K., Gupta, A., Balamurugan, R., Sriramurthy, V., Kumar, N.V. J. Org. Chem. (2006) [Pubmed]
  6. Investigation of the diastereoselectivity of tricyclo(5.2.1.0(2,6))decan-10-ones: controversies and agreements. Yadav, V.K., Singh, L. J. Org. Chem. (2005) [Pubmed]
  7. Silylmethyl-substituted aziridine and azetidine as masked 1,3- and 1,4-dipoles for formal [3 + 2] and [4 + 2] cycloaddition reactions. Yadav, V.K., Sriramurthy, V. J. Am. Chem. Soc. (2005) [Pubmed]
  8. Reactions on a solid surface. A simple, economical, and efficient acylation of alcohols and amines over Al2O3. Yadav, V.K., Ganesh Babu, K. J. Org. Chem. (2004) [Pubmed]
  9. Do the electronic effects of sulfur indeed control the pi-selectivity of gamma-sulfenyl Enones? An investigation. Yadav, V.K., Babu, K.G., Parvez, M. J. Org. Chem. (2004) [Pubmed]
  10. Highly stereoselective prins cyclization of silylmethyl-substituted cyclopropyl carbinols to 2,4,6-trisubstituted tetrahydropyrans. Yadav, V.K., Kumar, N.V. J. Am. Chem. Soc. (2004) [Pubmed]
  11. On the reaction of 1-oxa-4-thiaspiro[4.5]decan-7-one with PhLi. A reinvestigation. Yadav, V.K., Senthil, G., Singh, L., Parvez, M. J. Org. Chem. (2004) [Pubmed]
  12. Formal [3 + 2] and [3 + 3] additions of acceptor-substituted cyclopropylmethylsilanes to allenylsilanes. Yadav, V.K., Sriramurthy, V. Org. Lett. (2004) [Pubmed]
  13. Formal [3+2] addition of acceptor-substituted cyclopropylmethylsilanes with aryl acetylenes. Yadav, V.K., Sriramurthy, V. Angew. Chem. Int. Ed. Engl. (2004) [Pubmed]
  14. Diastereoselective aldol reactions of enolates generated from vicinally substituted trimethylsilylmethyl cyclopropyl ketones. Yadav, V.K., Balamurugan, R. Org. Lett. (2003) [Pubmed]
  15. 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. Yadav, V.K., Balamurugan, R. J. Org. Chem. (2002) [Pubmed]
  16. 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. Yadav, V.K., Senthil, G., Babu, K.G., Parvez, M., Reid, J.L. J. Org. Chem. (2002) [Pubmed]
  17. Synthesis of gamma-methylene oxacycles and alpha- and beta-alkylidene lactones via silicon-assisted ring opening of cyclopropyl carbinols. Yadav, V.K., Balamurugan, R. Chem. Commun. (Camb.) (2002) [Pubmed]
  18. Do the anti-selectivities of 2,3-endo,endo-dimethylnorbornan-7-one and the corresponding diethyl analog obey the cieplak model? An ab initio MO investigation and application of the cation complexation model. Yadav, V.K. J. Org. Chem. (2001) [Pubmed]
  19. Silicon-assisted ring opening of donor-acceptor substituted cyclopropanes. An expedient entry to substituted dihydrofurans. Yadav, V.K., Balamurugan, R. Org. Lett. (2001) [Pubmed]
 
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