The asymmetric Ullmann reaction III. Application of a first-order asymmetric transformation to the synthesis of C2-symmetric chiral, non-racemic biaryls-Reference-Cited by-同舟云学术

The asymmetric Ullmann reaction III. Application of a first-order asymmetric transformation to the synthesis of C2-symmetric chiral, non-racemic biaryls

Published:1994-05 Issue:20 Volume:35 Page:3259-3262
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Nelson Todd D.,Meyers A.I.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. Oxazoline-mediated biaryl coupling reactions. Stereocontrolled synthesis of 2,2′,6,6′-tetrasubstituted biphenyls.

2. An asymmetric synthesis of a C2 symmetric tetrasubstituted biaryl: 2,2′-Dihydroxy-6,6′-dimethyl-1,1′-biphenyl, a stable chiral system

3. A highly stereoselective synthesis of axially chiral biaryls. Application to the synthesis of a potential chiral catalysts.

4. Asymmetric total synthesis of dibenzocyclooctadiene lignans (-)-schizandrin and (-)-isoschizandrin. Structure revision of (+)-isoschizandrin

5. Synthesis of enantiomerically pure binaphthyl derivatives. Mechanism of the enantioselective, oxidative coupling of naphthols and designing a catalytic cycle

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