N-carbamoyl-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines(CAPP). Efficient new chiral ligands for asymmetric hydrogenation

Iwao Ojima; Noriko Yoda

doi:10.1016/S0040-4039(00)78836-8

N-carbamoyl-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines(CAPP). Efficient new chiral ligands for asymmetric hydrogenation

Iwao Ojima
, Noriko Yoda

Chemistry

Stony Brook University

Sagami Chemical Research Institute

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

35 Scopus citations

Abstract

A series of N-(N′-substituted carbamoyl)-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines (CAPP) was prepared, which exhibited excellent stereoselectivity in the asymmetric hydrogenation of α-acetamidocinnamic acid derivatives and itaconic acid as chiral ligand of the rhodium(I) catalyst.

Original language	English
Pages (from-to)	1051-1054
Number of pages	4
Journal	Tetrahedron Letters
Volume	21
Issue number	11
DOIs	https://doi.org/10.1016/S0040-4039(00)78836-8
State	Published - 1980

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title = "N-carbamoyl-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines(CAPP). Efficient new chiral ligands for asymmetric hydrogenation",

abstract = "A series of N-(N′-substituted carbamoyl)-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines (CAPP) was prepared, which exhibited excellent stereoselectivity in the asymmetric hydrogenation of α-acetamidocinnamic acid derivatives and itaconic acid as chiral ligand of the rhodium(I) catalyst.",

author = "Iwao Ojima and Noriko Yoda",

year = "1980",

doi = "10.1016/S0040-4039(00)78836-8",

language = "English",

volume = "21",

pages = "1051--1054",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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T1 - N-carbamoyl-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines(CAPP). Efficient new chiral ligands for asymmetric hydrogenation

AU - Ojima, Iwao

AU - Yoda, Noriko

PY - 1980

Y1 - 1980

N2 - A series of N-(N′-substituted carbamoyl)-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines (CAPP) was prepared, which exhibited excellent stereoselectivity in the asymmetric hydrogenation of α-acetamidocinnamic acid derivatives and itaconic acid as chiral ligand of the rhodium(I) catalyst.

AB - A series of N-(N′-substituted carbamoyl)-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines (CAPP) was prepared, which exhibited excellent stereoselectivity in the asymmetric hydrogenation of α-acetamidocinnamic acid derivatives and itaconic acid as chiral ligand of the rhodium(I) catalyst.

UR - https://www.scopus.com/pages/publications/0000285882

U2 - 10.1016/S0040-4039(00)78836-8

DO - 10.1016/S0040-4039(00)78836-8

M3 - Article

SN - 0040-4039

VL - 21

SP - 1051

EP - 1054

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 11

ER -

N-carbamoyl-4-diphenylphosphino-2-diphenylphosphinomethylpyrrolidines(CAPP). Efficient new chiral ligands for asymmetric hydrogenation

Abstract

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