An unusual approach to the synthesis of enantiomerically cis linear homoallylic alcohols based on the steric interaction mechanism of camphor scaffold

Chi Lik Ken Lee; Cheng Hsia Angeline Lee; Kui Thong Tan; Teck Peng Loh

doi:10.1021/ol049633z

An unusual approach to the synthesis of enantiomerically cis linear homoallylic alcohols based on the steric interaction mechanism of camphor scaffold

Chi Lik Ken Lee, Cheng Hsia Angeline Lee, Kui Thong Tan, Teck Peng Loh^*

^*Corresponding author for this work

National University of Singapore

Research output: Contribution to journal › Article › peer-review

57 Citations (Scopus)

Abstract

Camphor is used as the chiral auxiliary for the enantioselective synthesis of cis linear homoallylic alcohols. A range of catalysts, aldehydes, and solvents were investigated to obtain the optimum yield, enantioselectivity, and cis olefinic geometry.

Original language	English
Pages (from-to)	1281-1283
Number of pages	3
Journal	Organic Letters
Volume	6
Issue number	8
DOIs	https://doi.org/10.1021/ol049633z
Publication status	Published - Apr 15 2004
Externally published	Yes

ASJC Scopus Subject Areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol049633z

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abstract = "Camphor is used as the chiral auxiliary for the enantioselective synthesis of cis linear homoallylic alcohols. A range of catalysts, aldehydes, and solvents were investigated to obtain the optimum yield, enantioselectivity, and cis olefinic geometry.",

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AU - Loh, Teck Peng

PY - 2004/4/15

Y1 - 2004/4/15

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An unusual approach to the synthesis of enantiomerically cis linear homoallylic alcohols based on the steric interaction mechanism of camphor scaffold

Abstract

ASJC Scopus Subject Areas

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