Enantiomer separation of rac-2,2′-dihydroxy-1,1′-binaphthyl (BNO) by inclusion complexation with racemic or achiral ammonium salts and a novel transformation of a 1:1:1 racemic complex of BNO, Me4N+·Cl− and MeOH into a conglomerate complex in the solid state-Reference-Cited by-同舟云学术

Enantiomer separation of rac-2,2′-dihydroxy-1,1′-binaphthyl (BNO) by inclusion complexation with racemic or achiral ammonium salts and a novel transformation of a 1:1:1 racemic complex of BNO, Me4N+·Cl− and MeOH into a conglomerate complex in the solid state

Published:2004-08 Issue:35 Volume:60 Page:7767-7774
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Yoshizawa Kazuhiro,Toyota Shinji,Toda Fumio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Asymmetric synthesis via axially dissymmetric molecules. 6. Rational designing of efficient chiral reducing agents. Highly enantioselective reduction of aromatic ketones by binaphthol-modified lithium aluminum hydride reagents

2. Enantioselektive Addition von Arylgruppen an aromatische Aldehyde mit Aryltitan‐Binaphthol‐Derivaten

3. A model for metal-templated catalytic asymmetric induction via .pi.-allyl fragments

4. Studies on Enantioselective Addition of Chiral Titanium Reagents to Aromatic Aldehydes

5. Optical resolution of amine N-oxide by diastereoisomeric complex formation with optically active host compound

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