Transesterification of α-amino esters catalyzed by a tetranuclear zinc cluster: Zn 4(OCOCF 3) 6O

Yusuke Maegawa; Kazushi Agura; Yukiko Hayashi; Takashi Ohshima; Kazushi Mashima

doi:10.1055/s-0031-1290096

Transesterification of α-amino esters catalyzed by a tetranuclear zinc cluster: Zn ₄(OCOCF ₃) ₆O

Yusuke Maegawa, Kazushi Agura, Yukiko Hayashi, Takashi Ohshima, Kazushi Mashima

Chemo-Pharmaceutical Sciences

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

16 Citations (Scopus)

Abstract

Transesterification of amino acid ester derivatives was developed using a tetranuclear zinc cluster, Zn ₄(OCOCF ₃) ₆O, as the catalyst. Because the reaction conditions were very mild, a variety of N-protective groups and functional groups on side chains were tolerated.

Original language	English
Article number	U05911ST
Pages (from-to)	137-141
Number of pages	5
Journal	Synlett
Issue number	1
DOIs	https://doi.org/10.1055/s-0031-1290096
Publication status	Published - 2012

All Science Journal Classification (ASJC) codes

Organic Chemistry

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title = "Transesterification of α-amino esters catalyzed by a tetranuclear zinc cluster: Zn 4(OCOCF 3) 6O",

abstract = "Transesterification of amino acid ester derivatives was developed using a tetranuclear zinc cluster, Zn 4(OCOCF 3) 6O, as the catalyst. Because the reaction conditions were very mild, a variety of N-protective groups and functional groups on side chains were tolerated.",

author = "Yusuke Maegawa and Kazushi Agura and Yukiko Hayashi and Takashi Ohshima and Kazushi Mashima",

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AU - Agura, Kazushi

AU - Hayashi, Yukiko

AU - Ohshima, Takashi

AU - Mashima, Kazushi

PY - 2012

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AB - Transesterification of amino acid ester derivatives was developed using a tetranuclear zinc cluster, Zn 4(OCOCF 3) 6O, as the catalyst. Because the reaction conditions were very mild, a variety of N-protective groups and functional groups on side chains were tolerated.

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Transesterification of α-amino esters catalyzed by a tetranuclear zinc cluster: Zn ₄(OCOCF ₃) ₆O

Abstract

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