Asymmetric total synthesis of (+)-danicalipin A

Takehiko Yoshimitsu, Ryo Nakatani, Akihiro Kobayashi, Tetsuaki Tanaka

Research output: Contribution to journalArticle

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 languageEnglish
Pages (from-to)908-911
Number of pages4
JournalOrganic Letters
Volume13
Issue number5
DOIs
Publication statusPublished - Mar 4 2011
Externally publishedYes

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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

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 journalArticle

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, 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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