Catalytic enantioselective Strecker reaction of ketoimines using catalytic amount of TMSCN and stoichiometric amount of HCN
- 5 April 2004
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 45 (15) , 3153-3155
- https://doi.org/10.1016/j.tetlet.2004.02.077
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Catalytic Enantioselective Strecker Reactions and Analogous SynthesesChemical Reviews, 2003
- Catalytic Enantioselective Strecker Reaction of KetoiminesJournal of the American Chemical Society, 2003
- Structure-Based Analysis and Optimization of a Highly Enantioselective Catalyst for the Strecker ReactionJournal of the American Chemical Society, 2002
- Synthesis of Novel Quaternary Amino Acids Using Molybdenum-Catalyzed Asymmetric Allylic AlkylationJournal of the American Chemical Society, 2002
- Switching Enantiofacial Selectivities Using One Chiral Source: Catalytic Enantioselective Synthesis of the Key Intermediate for (20S)-Camptothecin Family by (S)-Selective Cyanosilylation of KetonesJournal of the American Chemical Society, 2001
- Sc(BINOL)2Li: a new heterobimetallic catalyst for the asymmetric Strecker reactionTetrahedron: Asymmetry, 2001
- Practical Catalytic Enantioselective Synthesis of α,α-Dialkyl-α-amino Acids by Chiral Phase-Transfer CatalysisJournal of the American Chemical Society, 2000
- The Atom Economy—A Search for Synthetic EfficiencyScience, 1991
- Alkylsilyl cyanides as silylating agentsThe Journal of Organic Chemistry, 1986
- Bromcyan und wasser‐freie BlausäureBerichte der deutschen chemischen Gesellschaft (A and B Series), 1934