Indium-mediated propargylation of aldehydes: Regioselectivity and enantioselectivity studies

Teck Peng Loh; Man Jing Lin; Kee Leng Tan

doi:10.1016/S0040-4039(02)02613-8

Indium-mediated propargylation of aldehydes: Regioselectivity and enantioselectivity studies

Teck Peng Loh^*, Man Jing Lin, Kee Leng Tan

^*Corresponding author for this work

National University of Singapore

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

65 Citations (Scopus)

Abstract

An enantioselective propargylation reaction of aldehydes with enantioselectivity up to 85% has been achieved in organic solvents by using stoichiometric amounts of (-)-cinchonidine as the chiral source.

Original language	English
Pages (from-to)	507-509
Number of pages	3
Journal	Tetrahedron Letters
Volume	44
Issue number	3
DOIs	https://doi.org/10.1016/S0040-4039(02)02613-8
Publication status	Published - Jan 13 2003
Externally published	Yes

ASJC Scopus Subject Areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(02)02613-8

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title = "Indium-mediated propargylation of aldehydes: Regioselectivity and enantioselectivity studies",

abstract = "An enantioselective propargylation reaction of aldehydes with enantioselectivity up to 85% has been achieved in organic solvents by using stoichiometric amounts of (-)-cinchonidine as the chiral source.",

author = "Loh, {Teck Peng} and Lin, {Man Jing} and Tan, {Kee Leng}",

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AU - Loh, Teck Peng

AU - Lin, Man Jing

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PY - 2003/1/13

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AB - An enantioselective propargylation reaction of aldehydes with enantioselectivity up to 85% has been achieved in organic solvents by using stoichiometric amounts of (-)-cinchonidine as the chiral source.

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JO - Tetrahedron Letters

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Indium-mediated propargylation of aldehydes: Regioselectivity and enantioselectivity studies

Abstract

ASJC Scopus Subject Areas

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