An asymmetric hydrogen equivalent: use of the 1-naphthylphenylmethylsilyl group in the preparation of optically active allyl alcohols and (S) 1-phenyl-1,2-butadiene.-Reference-Cited by-同舟云学术

An asymmetric hydrogen equivalent: use of the 1-naphthylphenylmethylsilyl group in the preparation of optically active allyl alcohols and (S) 1-phenyl-1,2-butadiene.

Published:1988-01 Issue:12 Volume:29 Page:1355-1358
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Torres Evelyn,Larson Gerald L.,McGarvey Glenn J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. (.alpha.-Haloethyl)silanes optically active at carbon and at silicon. Synthesis and absolute configuration

2. Asymmetric induction by chiral silicon groups

3. Silanes in organic synthesis. 19. Examination of (-)-.alpha.-naphthylphenylmethylallylsilane as a template for effecting chirality transfer from silicon to carbon

4. Silanes in organic synthesis. 18. Preparation and reactivity of optically active vinyl- and dienylsilanes

5. Optically active silyl- and germylmethyllithium reagents and the stereochemistry of carbene insertions into the silicon-hydrogen and germanium-hydrogen bonds

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