Synthetic approach to kendomycin: Preparation the C-glycosidic core

Tetsuya Sengoku; Hirokazu Arimoto; Daisuke Uemura

doi:10.1039/b402391a

Synthetic approach to kendomycin: Preparation the C-glycosidic core

Tetsuya Sengoku, Hirokazu Arimoto, Daisuke Uemura

LIF - Molecular and Chemical Life Science

Nagoya University

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

22 Citations (Scopus)

Abstract

Synthesis of the C13–C19 C-glycoside portion of kendomycin was achieved via oxidative pyran cyclization and Claisen rearrangement to construct the fully functionalized aromatic ring.

Original language	English
Pages (from-to)	1220-1221
Number of pages	2
Journal	Chemical Communications
Volume	4
Issue number	10
DOIs	https://doi.org/10.1039/b402391a
Publication status	Published - 2004

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abstract = "Synthesis of the C13–C19 C-glycoside portion of kendomycin was achieved via oxidative pyran cyclization and Claisen rearrangement to construct the fully functionalized aromatic ring.",

author = "Tetsuya Sengoku and Hirokazu Arimoto and Daisuke Uemura",

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AU - Sengoku, Tetsuya

AU - Arimoto, Hirokazu

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JO - Chemical Communications

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Synthetic approach to kendomycin: Preparation the C-glycosidic core

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