Year |
Citation |
Score |
2013 |
Delvos LB, Vyas DJ, Oestreich M. 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. PMID 23512610 DOI: 10.1002/Anie.201300648 |
0.661 |
|
2013 |
Dar BA, Chakraborty A, Sharma PR, Shrivastava V, Bhowmik A, Vyas D, Bhatti P, Sharma M, Singh B. 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. DOI: 10.1016/j.jiec.2012.10.018 |
0.338 |
|
2013 |
Delvos LB, Vyas DJ, Oestreich M. Asymmetrische Synthese α-chiraler Allylsilane durch enantiokonvergente γ-selektive Kupfer(I)-katalysierte allylische Silylierung Angewandte Chemie. 125: 4748-4751. DOI: 10.1002/Ange.201300648 |
0.617 |
|
2011 |
Kleeberg C, Feldmann E, Hartmann E, Vyas DJ, Oestreich M. Copper-catalyzed 1,2-addition of nucleophilic silicon to aldehydes: mechanistic insight and catalytic systems. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13538-43. PMID 22025369 DOI: 10.1002/Chem.201102367 |
0.66 |
|
2011 |
Vyas DJ, Hazra CK, Oestreich M. Copper(I)-catalyzed regioselective propargylic substitution involving Si-B bond activation. Organic Letters. 13: 4462-5. PMID 21786824 DOI: 10.1021/Ol201811D |
0.686 |
|
2011 |
Hartmann E, Vyas DJ, Oestreich M. Enantioselective formal hydration of α,β-unsaturated acceptors: asymmetric conjugate addition of silicon and boron nucleophiles. Chemical Communications (Cambridge, England). 47: 7917-32. PMID 21528142 DOI: 10.1039/C1Cc10528K |
0.654 |
|
2011 |
Vyas DJ, Fröhlich R, Oestreich M. Activation of the Si-B linkage: copper-catalyzed addition of nucleophilic silicon to imines. Organic Letters. 13: 2094-7. PMID 21417305 DOI: 10.1021/Ol200509C |
0.544 |
|
2010 |
Vyas DJ, Oestreich M. Copper-catalyzed Si-B bond activation in branched-selective allylic substitution of linear allylic chlorides. Angewandte Chemie (International Ed. in English). 49: 8513-5. PMID 20836116 DOI: 10.1002/Anie.201004658 |
0.568 |
|
2010 |
Vyas DJ, Fröhlich R, Oestreich M. Stereochemical surprises in the Lewis acid-mediated allylation of isatins. The Journal of Organic Chemistry. 75: 6720-3. PMID 20825233 DOI: 10.1021/Jo101420E |
0.517 |
|
2010 |
Vyas DJ, Oestreich M. Expedient access to branched allylic silanes by copper-catalysed allylic substitution of linear allylic halides. Chemical Communications (Cambridge, England). 46: 568-70. PMID 20062864 DOI: 10.1039/B920793G |
0.56 |
|
2010 |
Vyas DJ, Oestreich M. Kupferkatalysierte Si-B-Bindungsaktivierung in der verzweigtselektiven allylischen Substitution linearer Allylchloride Angewandte Chemie. 122: 8692-8694. DOI: 10.1002/Ange.201004658 |
0.434 |
|
Show low-probability matches. |