Selective preparation of optically pure (R,R)-1,1′:5′,1″-ternaphthalene-2,2′,6′,2″-tetraol: A new higher homolog of BINOL
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Centenary Lecture. Chemical multiplication of chirality: science and applications
2. C2 symmetry and asymmetric induction
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4. C-C Coupling reaction of 1,5-dibromo-2,6-dihydroxynaphthalene with alkali 2-naphthoxide. Opposite effects of counterion coordination and hydrogen bonding on stereoselectivity in the formation of cis- and trans-1,1′:5′,1″-ternaphthyls
5. Axial chirality control by 2,4-pentanediol or its analogue as a simple chiral linking bridge. Highly diastereodifferentiating homocoupling of a 1-lithio-2-naphthyl ether
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3. Miscellaneous Reactions;Key Chiral Auxiliary Applications;2014
4. Application ofD-chiro-Inositol as a Chiral Template for theDielsAlderReaction;Helvetica Chimica Acta;2012-10
5. ChemInform Abstract: Selective Preparation of Optically Pure (R,R)-1,1′:5′,1′′-Ternaphthalene-2,2′,6′,2′′-tetraol: A New Higher Homologue of BINOL.;ChemInform;2010-06-18
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