Enantioselective synthesis of attenols A and B

Kiyotake Suenaga; Keisuke Araki; Tetsuya Sengoku; Daisuke Uemura

doi:10.1021/ol006905z

Enantioselective synthesis of attenols A and B

Kiyotake Suenaga, Keisuke Araki, Tetsuya Sengoku, Daisuke Uemura

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

50 Citations (Scopus)

Abstract

(Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.

Original language	English
Pages (from-to)	527-529
Number of pages	3
Journal	Organic Letters
Volume	3
Issue number	4
DOIs	https://doi.org/10.1021/ol006905z
Publication status	Published - 2001 Feb 22
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol006905z

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title = "Enantioselective synthesis of attenols A and B",

abstract = "(Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.",

author = "Kiyotake Suenaga and Keisuke Araki and Tetsuya Sengoku and Daisuke Uemura",

year = "2001",

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journal = "Organic Letters",

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T1 - Enantioselective synthesis of attenols A and B

AU - Suenaga, Kiyotake

AU - Araki, Keisuke

AU - Sengoku, Tetsuya

AU - Uemura, Daisuke

PY - 2001/2/22

Y1 - 2001/2/22

N2 - (Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.

AB - (Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.

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U2 - 10.1021/ol006905z

DO - 10.1021/ol006905z

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JO - Organic Letters

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Enantioselective synthesis of attenols A and B

Abstract

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