New and Efficient Synthesis of Azabicyclo[4.4.0]alkane Amino Acids by Rh-Catalyzed Cyclohydrocarbonylation

Nobuhiro Mizutani; Wen Hua Chiou; Iwao Ojima

doi:10.1021/ol026782d

New and Efficient Synthesis of Azabicyclo[4.4.0]alkane Amino Acids by Rh-Catalyzed Cyclohydrocarbonylation

Nobuhiro Mizutani
, Wen Hua Chiou
, Iwao Ojima

Chemistry

Stony Brook University
Kirin Holdings Co., Ltd.

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

38 Scopus citations

Abstract

(Matrix Presented) Highly efficient syntheses of azabicyclo[4.4.0]alkane amino acids were achieved by Rh-catalyzed cyclohydrocarbonylation of dipeptides bearing a terminal olefin moiety and a heteroatom nucleophile.

Original language	English
Pages (from-to)	4575-4578
Number of pages	4
Journal	Organic Letters
Volume	4
Issue number	26
DOIs	https://doi.org/10.1021/ol026782d
State	Published - Dec 26 2002

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@article{89df91b85ae04fcc81e6e9be728d271a,

title = "New and Efficient Synthesis of Azabicyclo[4.4.0]alkane Amino Acids by Rh-Catalyzed Cyclohydrocarbonylation",

abstract = "(Matrix Presented) Highly efficient syntheses of azabicyclo[4.4.0]alkane amino acids were achieved by Rh-catalyzed cyclohydrocarbonylation of dipeptides bearing a terminal olefin moiety and a heteroatom nucleophile.",

author = "Nobuhiro Mizutani and Chiou, \{Wen Hua\} and Iwao Ojima",

year = "2002",

month = dec,

day = "26",

doi = "10.1021/ol026782d",

language = "English",

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journal = "Organic Letters",

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T1 - New and Efficient Synthesis of Azabicyclo[4.4.0]alkane Amino Acids by Rh-Catalyzed Cyclohydrocarbonylation

AU - Mizutani, Nobuhiro

AU - Chiou, Wen Hua

AU - Ojima, Iwao

PY - 2002/12/26

Y1 - 2002/12/26

N2 - (Matrix Presented) Highly efficient syntheses of azabicyclo[4.4.0]alkane amino acids were achieved by Rh-catalyzed cyclohydrocarbonylation of dipeptides bearing a terminal olefin moiety and a heteroatom nucleophile.

AB - (Matrix Presented) Highly efficient syntheses of azabicyclo[4.4.0]alkane amino acids were achieved by Rh-catalyzed cyclohydrocarbonylation of dipeptides bearing a terminal olefin moiety and a heteroatom nucleophile.

UR - https://www.scopus.com/pages/publications/0141826237

U2 - 10.1021/ol026782d

DO - 10.1021/ol026782d

M3 - Article

C2 - 12489933

AN - SCOPUS:0141826237

SN - 1523-7060

VL - 4

SP - 4575

EP - 4578

JO - Organic Letters

JF - Organic Letters

IS - 26

ER -

New and Efficient Synthesis of Azabicyclo[4.4.0]alkane Amino Acids by Rh-Catalyzed Cyclohydrocarbonylation

Abstract

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