Total synthesis of (±)-lysidicin A

Yusuke Ogura; Ken Ishigami; Hidenori Watanabe

doi:10.1016/j.tet.2011.12.062

Total synthesis of (±)-lysidicin A

Yusuke Ogura, Ken Ishigami, Hidenori Watanabe

AGR - Bioscience and Biotechnology for Future Bioindustries

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7 Citations (Scopus)

Abstract

Lysidicin A, which has been isolated from Lisidicie rhodostegia possesses complicated structure. A total synthesis of lysidicin A has been achieved and is described herein. The key reaction is single and cascade Claisen rearrangements.

Original language	English
Pages (from-to)	1723-1728
Number of pages	6
Journal	Tetrahedron
Volume	68
Issue number	6
DOIs	https://doi.org/10.1016/j.tet.2011.12.062
Publication status	Published - 2012 Feb 11

Keywords

Acetal
Cascade reaction
Claisen rearrangement
Lysidicin A
Total synthesis

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "Total synthesis of (±)-lysidicin A",

abstract = "Lysidicin A, which has been isolated from Lisidicie rhodostegia possesses complicated structure. A total synthesis of lysidicin A has been achieved and is described herein. The key reaction is single and cascade Claisen rearrangements.",

keywords = "Acetal, Cascade reaction, Claisen rearrangement, Lysidicin A, Total synthesis",

author = "Yusuke Ogura and Ken Ishigami and Hidenori Watanabe",

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AU - Ogura, Yusuke

AU - Ishigami, Ken

AU - Watanabe, Hidenori

PY - 2012/2/11

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N2 - Lysidicin A, which has been isolated from Lisidicie rhodostegia possesses complicated structure. A total synthesis of lysidicin A has been achieved and is described herein. The key reaction is single and cascade Claisen rearrangements.

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KW - Claisen rearrangement

KW - Lysidicin A

KW - Total synthesis

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JF - Tetrahedron

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