A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium

Teck Peng Loh; Jian Rong Zhou

doi:10.1016/S0040-4039(00)00801-7

A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium

Teck Peng Loh^*, Jian Rong Zhou

^*Corresponding author for this work

National University of Singapore

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

65 Citations (Scopus)

Abstract

A modified Yamamoto-Yanagisawa's catalyst (S)-Tol-BINAP·AgNO₃ was successfully applied to a catalytic enantioselective allylation reaction of aldehydes in an aqueous system. The reactions with aromatic aldehydes afforded the desired products in high yields with good stereoselectivities. (C) 2000 Published by Elsevier Science Ltd.

Original language	English
Pages (from-to)	5261-5264
Number of pages	4
Journal	Tetrahedron Letters
Volume	41
Issue number	27
DOIs	https://doi.org/10.1016/S0040-4039(00)00801-7
Publication status	Published - Jul 1 2000
Externally published	Yes

ASJC Scopus Subject Areas

Biochemistry
Drug Discovery
Organic Chemistry

Keywords

Aldehyde
Allylation
Aqueous
Catalyst
Enantioselectivity

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10.1016/S0040-4039(00)00801-7

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abstract = "A modified Yamamoto-Yanagisawa's catalyst (S)-Tol-BINAP·AgNO3 was successfully applied to a catalytic enantioselective allylation reaction of aldehydes in an aqueous system. The reactions with aromatic aldehydes afforded the desired products in high yields with good stereoselectivities. (C) 2000 Published by Elsevier Science Ltd.",

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author = "Loh, {Teck Peng} and Zhou, {Jian Rong}",

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T1 - A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium

AU - Loh, Teck Peng

AU - Zhou, Jian Rong

PY - 2000/7/1

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N2 - A modified Yamamoto-Yanagisawa's catalyst (S)-Tol-BINAP·AgNO3 was successfully applied to a catalytic enantioselective allylation reaction of aldehydes in an aqueous system. The reactions with aromatic aldehydes afforded the desired products in high yields with good stereoselectivities. (C) 2000 Published by Elsevier Science Ltd.

AB - A modified Yamamoto-Yanagisawa's catalyst (S)-Tol-BINAP·AgNO3 was successfully applied to a catalytic enantioselective allylation reaction of aldehydes in an aqueous system. The reactions with aromatic aldehydes afforded the desired products in high yields with good stereoselectivities. (C) 2000 Published by Elsevier Science Ltd.

KW - Aldehyde

KW - Allylation

KW - Aqueous

KW - Catalyst

KW - Enantioselectivity

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U2 - 10.1016/S0040-4039(00)00801-7

DO - 10.1016/S0040-4039(00)00801-7

M3 - Article

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 27

ER -

A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium

Abstract

ASJC Scopus Subject Areas

Keywords

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