Total synthesis of preswinholide A. 2. Completion of the synthesis

Kazuo Nagasawa; Isao Shimizu; Tadashi Nakata

doi:10.1016/0040-4039(96)01504-3

Total synthesis of preswinholide A. 2. Completion of the synthesis

Kazuo Nagasawa, Isao Shimizu, Tadashi Nakata^*

^*この研究の対応する著者

研究成果: Article › 査読

16 被引用数 (Scopus)

抄録

Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.

本文言語	English
ページ（範囲）	6885-6888
ページ数	4
ジャーナル	Tetrahedron Letters
巻	37
号	38
DOI	https://doi.org/10.1016/0040-4039(96)01504-3
出版ステータス	Published - 1996 9月 16

ASJC Scopus subject areas

生化学
有機化学
創薬

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10.1016/0040-4039(96)01504-3

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title = "Total synthesis of preswinholide A. 2. Completion of the synthesis",

abstract = "Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.",

author = "Kazuo Nagasawa and Isao Shimizu and Tadashi Nakata",

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AU - Nagasawa, Kazuo

AU - Shimizu, Isao

AU - Nakata, Tadashi

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Y1 - 1996/9/16

N2 - Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.

AB - Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.

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U2 - 10.1016/0040-4039(96)01504-3

DO - 10.1016/0040-4039(96)01504-3

M3 - Article

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SP - 6885

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

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Total synthesis of preswinholide A. 2. Completion of the synthesis

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