Asymmetric hydrogenation of dehydroamino acid derivatives catalyzed by a new aminophosphine phosphinite ligand derived from ketopinic acid

Xingshu Li; Rongliang Lou; Chi Hung Yeung; Albert S.C. Chan; Rick W K WONG

doi:10.1016/S0957-4166(00)00164-6

Asymmetric hydrogenation of dehydroamino acid derivatives catalyzed by a new aminophosphine phosphinite ligand derived from ketopinic acid

Xingshu Li, Rongliang Lou, Chi Hung Yeung, Albert S.C. Chan^*, Rick W K WONG

^*Corresponding author for this work

Department of Chemistry

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

28 Citations (Scopus)

Abstract

A new chiral aminophosphine phosphinite N,O-bis(diphenylphosphino)-(1S,2R)-1-(N-methylamino) methyl-2-hydroxyl-7,7-dimethylbicyclo[2.2.1]heptane was synthesized from ketopinic acid and its application to the asymmetric hydrogenation of dehydroamino acid derivatives examined. Copyright (C) 2000 Elsevier Science Ltd.

Original language	English
Pages (from-to)	2077-2082
Number of pages	6
Journal	Tetrahedron Asymmetry
Volume	11
Issue number	10
DOIs	https://doi.org/10.1016/S0957-4166(00)00164-6
Publication status	Published - 2 Jun 2000

Scopus Subject Areas

Catalysis
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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title = "Asymmetric hydrogenation of dehydroamino acid derivatives catalyzed by a new aminophosphine phosphinite ligand derived from ketopinic acid",

abstract = "A new chiral aminophosphine phosphinite N,O-bis(diphenylphosphino)-(1S,2R)-1-(N-methylamino) methyl-2-hydroxyl-7,7-dimethylbicyclo[2.2.1]heptane was synthesized from ketopinic acid and its application to the asymmetric hydrogenation of dehydroamino acid derivatives examined. Copyright (C) 2000 Elsevier Science Ltd.",

author = "Xingshu Li and Rongliang Lou and Yeung, {Chi Hung} and Chan, {Albert S.C.} and WONG, {Rick W K}",

note = "Funding Information: We thank the Hong Kong Polytechnic University ASD fund and the Research Grants Council of Hong Kong (project number ERB003) for financial support of this study. ",

year = "2000",

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doi = "10.1016/S0957-4166(00)00164-6",

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T1 - Asymmetric hydrogenation of dehydroamino acid derivatives catalyzed by a new aminophosphine phosphinite ligand derived from ketopinic acid

AU - Li, Xingshu

AU - Lou, Rongliang

AU - Yeung, Chi Hung

AU - Chan, Albert S.C.

AU - WONG, Rick W K

N1 - Funding Information: We thank the Hong Kong Polytechnic University ASD fund and the Research Grants Council of Hong Kong (project number ERB003) for financial support of this study.

PY - 2000/6/2

Y1 - 2000/6/2

N2 - A new chiral aminophosphine phosphinite N,O-bis(diphenylphosphino)-(1S,2R)-1-(N-methylamino) methyl-2-hydroxyl-7,7-dimethylbicyclo[2.2.1]heptane was synthesized from ketopinic acid and its application to the asymmetric hydrogenation of dehydroamino acid derivatives examined. Copyright (C) 2000 Elsevier Science Ltd.

AB - A new chiral aminophosphine phosphinite N,O-bis(diphenylphosphino)-(1S,2R)-1-(N-methylamino) methyl-2-hydroxyl-7,7-dimethylbicyclo[2.2.1]heptane was synthesized from ketopinic acid and its application to the asymmetric hydrogenation of dehydroamino acid derivatives examined. Copyright (C) 2000 Elsevier Science Ltd.

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U2 - 10.1016/S0957-4166(00)00164-6

DO - 10.1016/S0957-4166(00)00164-6

M3 - Article

AN - SCOPUS:0034595631

SN - 0957-4166

VL - 11

SP - 2077

EP - 2082

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 10

ER -

Asymmetric hydrogenation of dehydroamino acid derivatives catalyzed by a new aminophosphine phosphinite ligand derived from ketopinic acid

Abstract

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