Asymmetric total synthesis of (+)-danicalipin A

Takehiko Yoshimitsu; Ryo Nakatani; Akihiro Kobayashi; Tetsuaki Tanaka

doi:10.1021/ol1029518

Asymmetric total synthesis of (+)-danicalipin A

Takehiko Yoshimitsu, Ryo Nakatani, Akihiro Kobayashi, Tetsuaki Tanaka

研究成果 › 査読

49 被引用数 (Scopus)

抄録

A convergent asymmetric total synthesis of (+)-danicalipin A is accomplished, in which two chlorinated fragments are stereoselectively joined by 1,3-dipolar coupling, leading to the confirmation of the absolute configuration of the natural product.(Figure Presented)

本文言語	English
ページ（範囲）	908-911
ページ数	4
ジャーナル	Organic Letters
巻	13
号	5
DOI	https://doi.org/10.1021/ol1029518
出版ステータス	Published - 3月 4 2011
外部発表	はい

ASJC Scopus subject areas

生化学
物理化学および理論化学
有機化学

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10.1021/ol1029518

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title = "Asymmetric total synthesis of (+)-danicalipin A",

abstract = "A convergent asymmetric total synthesis of (+)-danicalipin A is accomplished, in which two chlorinated fragments are stereoselectively joined by 1,3-dipolar coupling, leading to the confirmation of the absolute configuration of the natural product.(Figure Presented)",

author = "Takehiko Yoshimitsu and Ryo Nakatani and Akihiro Kobayashi and Tetsuaki Tanaka",

year = "2011",

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AU - Yoshimitsu, Takehiko

AU - Nakatani, Ryo

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PY - 2011/3/4

Y1 - 2011/3/4

N2 - A convergent asymmetric total synthesis of (+)-danicalipin A is accomplished, in which two chlorinated fragments are stereoselectively joined by 1,3-dipolar coupling, leading to the confirmation of the absolute configuration of the natural product.(Figure Presented)

AB - A convergent asymmetric total synthesis of (+)-danicalipin A is accomplished, in which two chlorinated fragments are stereoselectively joined by 1,3-dipolar coupling, leading to the confirmation of the absolute configuration of the natural product.(Figure Presented)

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Asymmetric total synthesis of (+)-danicalipin A

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