Kuldeep Wadhwa, Ph.D. - Publications
Affiliations: | 2009 | Chemistry | Iowa State University, Ames, IA, United States |
Area:
Novel Green Catalysts for Organic Reactions, Organometallic Self-Assembled SystemsYear | Citation | Score | |||
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2011 | Chintareddy VR, Wadhwa K, Verkade JG. Tetrabutylammonium fluoride (TBAF)-catalyzed addition of substituted trialkylsilylalkynes to aldehydes, ketones, and trifluoromethyl ketones. The Journal of Organic Chemistry. 76: 4482-8. PMID 21517057 DOI: 10.1021/Jo200314G | 0.561 | |||
2009 | Chintareddy VR, Wadhwa K, Verkade JG. P(PhCH2NCH2CH2)3N catalysis of Mukaiyama aldol reactions of aliphatic, aromatic, and heterocyclic aldehydes and trifluoromethyl phenyl ketone. The Journal of Organic Chemistry. 74: 8118-32. PMID 19795856 DOI: 10.1021/Jo901571Y | 0.604 | |||
2009 | Wadhwa K, Chintareddy VR, Verkade JG. P(PhCH(2)NCH(2)CH(2))(3)N: an efficient lewis base catalyst for the synthesis of propargylic alcohols and Morita-Baylis-Hillman adducts via aldehyde alkynylation. The Journal of Organic Chemistry. 74: 6681-90. PMID 19711995 DOI: 10.1021/Jo9012332 | 0.586 | |||
2009 | Wadhwa K, Verkade JG. P(i-PrNCH2CH2)3N as a Lewis base catalyst for the synthesis of beta-hydroxynitriles using TMSAN. The Journal of Organic Chemistry. 74: 5683-6. PMID 19555093 DOI: 10.1021/Jo900814T | 0.607 | |||
2009 | Wadhwa K, Verkade JG. P(i-PrNCH2CH2)3N: efficient catalyst for synthesizing beta-hydroxyesters and alpha,beta-unsaturated esters using alpha-trimethylsilylethylacetate (TMSEA). The Journal of Organic Chemistry. 74: 4368-71. PMID 19402695 DOI: 10.1021/Jo900477Q | 0.556 | |||
2009 | Kong X, Wadhwa K, Verkade JG, Schmidt-Rohr K. Determination of the structure of a novel anion exchange fuel cell membrane by solid-state nuclear magnetic resonance spectroscopy Macromolecules. 42: 1659-1664. DOI: 10.1021/Ma802613K | 0.404 | |||
2009 | Wadhwa K, Verkade JG. P(i-PrNCH2CH2)3N: an efficient catalyst for TMS-1,3-dithiane addition to aldehydes Tetrahedron Letters. 50: 4307-4309. DOI: 10.1016/J.Tetlet.2009.05.010 | 0.585 | |||
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