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

Research output: Contribution to journal › Article

42 Citations (Scopus)

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)

Original language	English
Pages (from-to)	908-911
Number of pages	4
Journal	Organic Letters
Volume	13
Issue number	5
DOIs	https://doi.org/10.1021/ol1029518
Publication status	Published - Mar 4 2011
Externally published	Yes

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Biological Products

fragments

synthesis

products

configurations

danicalipin A

ASJC Scopus subject areas

Organic Chemistry
Physical and Theoretical Chemistry
Biochemistry

Cite this

Yoshimitsu, T., Nakatani, R., Kobayashi, A., & Tanaka, T. (2011). Asymmetric total synthesis of (+)-danicalipin A. Organic Letters, 13(5), 908-911. https://doi.org/10.1021/ol1029518

Asymmetric total synthesis of (+)-danicalipin A. / Yoshimitsu, Takehiko; Nakatani, Ryo; Kobayashi, Akihiro; Tanaka, Tetsuaki.

In: Organic Letters, Vol. 13, No. 5, 04.03.2011, p. 908-911.

Research output: Contribution to journal › Article

Yoshimitsu, T, Nakatani, R, Kobayashi, A & Tanaka, T 2011, 'Asymmetric total synthesis of (+)-danicalipin A', Organic Letters, vol. 13, no. 5, pp. 908-911. https://doi.org/10.1021/ol1029518

Yoshimitsu T, Nakatani R, Kobayashi A, Tanaka T. Asymmetric total synthesis of (+)-danicalipin A. Organic Letters. 2011 Mar 4;13(5):908-911. https://doi.org/10.1021/ol1029518

Yoshimitsu, Takehiko ; Nakatani, Ryo ; Kobayashi, Akihiro ; Tanaka, Tetsuaki. / Asymmetric total synthesis of (+)-danicalipin A. In: Organic Letters. 2011 ; Vol. 13, No. 5. pp. 908-911.

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Access to Document

10.1021/ol1029518