Elaboration of a novel effective approach to enantiopure functionalised 2,2′-dialkyl-1,1′-binaphthyls by stereoconservative cross-couplings at positions 2 and 2′-Reference-Cited by-同舟云学术

Elaboration of a novel effective approach to enantiopure functionalised 2,2′-dialkyl-1,1′-binaphthyls by stereoconservative cross-couplings at positions 2 and 2′

Published:2004-06 Issue:27 Volume:45 Page:5279-5282
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kasák Peter,Putala Martin

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

1. Molecular Design of a C2-Symmetric Chiral Phase-Transfer Catalyst for Practical Asymmetric Synthesis of α-Amino Acids

2. Synthesis and Application of the First Chiral and Highly Lewis Acidic Silyl Cationic Catalyst

3. Clarification of the Nature of the “First Chiral and Highly Lewis Acidic Silyl Cationic Catalyst”. Concerning the Question of Siliconium Ions vs Silyl Cations1

4. Nonenzymatic Kinetic Resolution of 1,2-Diols Catalyzed by an Organotin Compound

5. Chemo- and Stereoselective Monobenzoylation of 1,2-Diols Catalyzed by Organotin Compounds

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