A new stereoselective route to (-)-octalactin A based on intramolecular SmI2 promoted Reformatsky reaction

Susumu Inoue; Yoshiharu Iwabuchi; Hiroshi Irie; Susumi Hatakeyama

doi:10.1055/s-1998-1778

A new stereoselective route to (-)-octalactin A based on intramolecular SmI₂ promoted Reformatsky reaction

Susumu Inoue, Yoshiharu Iwabuchi, Hiroshi Irie, Susumi Hatakeyama

研究成果: Article › 査読

25 被引用数 (Scopus)

抄録

A novel stereoselective synthesis of the key left-hand fragment of (-)-octalactin A has been achieved from methyl (R)-3-hydroxy-2-methylpropionate employing SmI₂ promoted intramolecular Reformatsky reaction of a δ-(bromoacetoxy)aldehyde as a key step.

本文言語	English
ページ（範囲）	735-736
ページ数	2
ジャーナル	Synlett
号	7
DOI	https://doi.org/10.1055/s-1998-1778
出版ステータス	Published - 1998 7月
外部発表	はい

ASJC Scopus subject areas

有機化学

文献へのアクセス

10.1055/s-1998-1778

他のファイルとリンク

引用スタイル

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