Total synthesis of preswinholide A. 1. Stereoselective synthesis of the C11-C23 segment

Kazuo Nagasawa; Isao Shimizu; Tadashi Nakata

doi:10.1016/0040-4039(96)01503-1

Total synthesis of preswinholide A. 1. Stereoselective synthesis of the C11-C23 segment

Kazuo Nagasawa, Isao Shimizu, Tadashi Nakata^*

^*この研究の対応する著者

研究成果: Article › 査読

22 被引用数 (Scopus)

抄録

The C11-C23 segment of preswinholide A was stereoselectively synthesized based on the iterative construction of 1,3-polyol chains using a series of sequential reactions which involves the Sharpless asymmetric epoxidation of allyl alcohol and Pd-catalyzed hydrogenolysis of alkenyl oxirane with HCOOH as the key reactions.

本文言語	English
ページ（範囲）	6881-6884
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)01503-1
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)01503-1

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title = "Total synthesis of preswinholide A. 1. Stereoselective synthesis of the C11-C23 segment",

abstract = "The C11-C23 segment of preswinholide A was stereoselectively synthesized based on the iterative construction of 1,3-polyol chains using a series of sequential reactions which involves the Sharpless asymmetric epoxidation of allyl alcohol and Pd-catalyzed hydrogenolysis of alkenyl oxirane with HCOOH as the key reactions.",

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

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AU - Nakata, Tadashi

PY - 1996/9/16

Y1 - 1996/9/16

N2 - The C11-C23 segment of preswinholide A was stereoselectively synthesized based on the iterative construction of 1,3-polyol chains using a series of sequential reactions which involves the Sharpless asymmetric epoxidation of allyl alcohol and Pd-catalyzed hydrogenolysis of alkenyl oxirane with HCOOH as the key reactions.

AB - The C11-C23 segment of preswinholide A was stereoselectively synthesized based on the iterative construction of 1,3-polyol chains using a series of sequential reactions which involves the Sharpless asymmetric epoxidation of allyl alcohol and Pd-catalyzed hydrogenolysis of alkenyl oxirane with HCOOH as the key reactions.

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JO - Tetrahedron Letters

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Total synthesis of preswinholide A. 1. Stereoselective synthesis of the C11-C23 segment

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