Dynamic kinetic resolution in BINAP-ruthenium(II) catalyzed hydrogenation of 2-substituted 3-oxo carboxylic esters

M. Kitamura; T. Ohkuma; M. Tokunaga; R. Noyori

doi:10.1016/S0957-4166(00)82262-4

Dynamic kinetic resolution in BINAP-ruthenium(II) catalyzed hydrogenation of 2-substituted 3-oxo carboxylic esters

M. Kitamura, T. Ohkuma, M. Tokunaga, R. Noyori

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

97 Citations (Scopus)

Abstract

BINAP-Ru catalyzed hydrogenation allows efficient dynamic kinetic resolution of certain 2-substituted 3-oxo carboxylic esters having cyclic structures to lead to the alcoholic products in high enantiomeric and diastereomeric excesses.

Original language	English
Pages (from-to)	1-4
Number of pages	4
Journal	Tetrahedron: Asymmetry
Volume	1
Issue number	1
DOIs	https://doi.org/10.1016/S0957-4166(00)82262-4
Publication status	Published - 1990
Externally published	Yes

All Science Journal Classification (ASJC) codes

Catalysis
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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10.1016/S0957-4166(00)82262-4

Cite this

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title = "Dynamic kinetic resolution in BINAP-ruthenium(II) catalyzed hydrogenation of 2-substituted 3-oxo carboxylic esters",

abstract = "BINAP-Ru catalyzed hydrogenation allows efficient dynamic kinetic resolution of certain 2-substituted 3-oxo carboxylic esters having cyclic structures to lead to the alcoholic products in high enantiomeric and diastereomeric excesses.",

author = "M. Kitamura and T. Ohkuma and M. Tokunaga and R. Noyori",

year = "1990",

doi = "10.1016/S0957-4166(00)82262-4",

language = "English",

volume = "1",

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journal = "Tetrahedron: Asymmetry",

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T1 - Dynamic kinetic resolution in BINAP-ruthenium(II) catalyzed hydrogenation of 2-substituted 3-oxo carboxylic esters

AU - Kitamura, M.

AU - Ohkuma, T.

AU - Tokunaga, M.

AU - Noyori, R.

PY - 1990

Y1 - 1990

N2 - BINAP-Ru catalyzed hydrogenation allows efficient dynamic kinetic resolution of certain 2-substituted 3-oxo carboxylic esters having cyclic structures to lead to the alcoholic products in high enantiomeric and diastereomeric excesses.

AB - BINAP-Ru catalyzed hydrogenation allows efficient dynamic kinetic resolution of certain 2-substituted 3-oxo carboxylic esters having cyclic structures to lead to the alcoholic products in high enantiomeric and diastereomeric excesses.

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U2 - 10.1016/S0957-4166(00)82262-4

DO - 10.1016/S0957-4166(00)82262-4

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AN - SCOPUS:0001773245

SN - 0957-4166

VL - 1

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JO - Tetrahedron: Asymmetry

JF - Tetrahedron: Asymmetry

IS - 1

ER -

Dynamic kinetic resolution in BINAP-ruthenium(II) catalyzed hydrogenation of 2-substituted 3-oxo carboxylic esters

Abstract

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