Regioselective lactonization of unsymmetrical 1,4-diols: An efficient access to lactone lignans

Masato Ito; Akira Shiibashi; Takao Ikariya

doi:10.1039/c0cc04926c

Regioselective lactonization of unsymmetrical 1,4-diols: An efficient access to lactone lignans

Masato Ito
, Akira Shiibashi
, Takao Ikariya

分子集積化学部門

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

19 被引用数 (Scopus)

抄録

A Cp*Ru-based bifunctional catalyst system (Cp* = η⁵-C₅(CH₃)₅) with a suitably-designed PN ligand (PN = chelating tertiary phosphine-protic amine ligand) has been developed for a regioselective lactonization of unsymmetrically substituted 1,4-diols, which may provide an expeditious access to a variety of lactone lignans.

本文言語	英語
ページ（範囲）	2134-2136
ページ数	3
ジャーナル	Chemical Communications
巻	47
号	7
DOI	https://doi.org/10.1039/c0cc04926c
出版ステータス	出版済み - 2月 1 2011

!!!All Science Journal Classification (ASJC) codes

電子材料、光学材料、および磁性材料
触媒
セラミックおよび複合材料
化学一般
表面、皮膜および薄膜
金属および合金
材料化学

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abstract = "A Cp*Ru-based bifunctional catalyst system (Cp* = η5-C5(CH3)5) with a suitably-designed PN ligand (PN = chelating tertiary phosphine-protic amine ligand) has been developed for a regioselective lactonization of unsymmetrically substituted 1,4-diols, which may provide an expeditious access to a variety of lactone lignans.",

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AU - Shiibashi, Akira

AU - Ikariya, Takao

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AB - A Cp*Ru-based bifunctional catalyst system (Cp* = η5-C5(CH3)5) with a suitably-designed PN ligand (PN = chelating tertiary phosphine-protic amine ligand) has been developed for a regioselective lactonization of unsymmetrically substituted 1,4-diols, which may provide an expeditious access to a variety of lactone lignans.

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Regioselective lactonization of unsymmetrical 1,4-diols: An efficient access to lactone lignans

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!!!All Science Journal Classification (ASJC) codes

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