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; Wai Kwok 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^*
, Wai Kwok Wong

^*Corresponding author for this work

Research output: Contribution to journal › 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

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@article{e61e2d6d33034a87ae6b29314ebad8b6,

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, \{Wai Kwok\}",

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. Publisher copyright: {\textcopyright} 2000 Elsevier Science Ltd.",

year = "2000",

month = jun,

day = "2",

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

language = "English",

volume = "11",

pages = "2077--2082",

journal = "Tetrahedron Asymmetry",

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TY - JOUR

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, Wai Kwok

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. Publisher copyright: © 2000 Elsevier Science Ltd.

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.

UR - https://www.scopus.com/pages/publications/0034595631

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

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

M3 - Journal 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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