Devendra Vyas

2008-2011 Westfälische Wilhelms-Universität Münster, Münster, Nordrhein-Westfalen, Germany 
"Devendra Vyas"
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Delvos LB, Vyas DJ, Oestreich M. (2013) Asymmetric synthesis of α-chiral allylic silanes by enantioconvergent γ-selective copper(I)-catalyzed allylic silylation. Angewandte Chemie (International Ed. in English). 52: 4650-3
Dar BA, Chakraborty A, Sharma PR, et al. (2013) Grinding-induced rapid, convenient and solvent free approach for the one pot synthesis of α-aminophosphonates using aluminium pillared interlayered clay catalyst Journal of Industrial and Engineering Chemistry. 19: 732-738
Delvos LB, Vyas DJ, Oestreich M. (2013) Asymmetrische Synthese α-chiraler Allylsilane durch enantiokonvergente γ-selektive Kupfer(I)-katalysierte allylische Silylierung Angewandte Chemie. 125: 4748-4751
Kleeberg C, Feldmann E, Hartmann E, et al. (2011) Copper-catalyzed 1,2-addition of nucleophilic silicon to aldehydes: mechanistic insight and catalytic systems. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13538-43
Vyas DJ, Hazra CK, Oestreich M. (2011) Copper(I)-catalyzed regioselective propargylic substitution involving Si-B bond activation. Organic Letters. 13: 4462-5
Hartmann E, Vyas DJ, Oestreich M. (2011) Enantioselective formal hydration of α,β-unsaturated acceptors: asymmetric conjugate addition of silicon and boron nucleophiles. Chemical Communications (Cambridge, England). 47: 7917-32
Vyas DJ, Fröhlich R, Oestreich M. (2011) Activation of the Si-B linkage: copper-catalyzed addition of nucleophilic silicon to imines. Organic Letters. 13: 2094-7
Vyas DJ, Oestreich M. (2010) Copper-catalyzed Si-B bond activation in branched-selective allylic substitution of linear allylic chlorides. Angewandte Chemie (International Ed. in English). 49: 8513-5
Vyas DJ, Fröhlich R, Oestreich M. (2010) Stereochemical surprises in the Lewis acid-mediated allylation of isatins. The Journal of Organic Chemistry. 75: 6720-3
Vyas DJ, Oestreich M. (2010) Expedient access to branched allylic silanes by copper-catalysed allylic substitution of linear allylic halides. Chemical Communications (Cambridge, England). 46: 568-70
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