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 › peer-review

46 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

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

Access to Document

10.1021/ol1029518

Cite this

@article{6b230bc2daca43f4b7f25c0ee7c28c65,

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",

month = mar,

day = "4",

doi = "10.1021/ol1029518",

language = "English",

volume = "13",

pages = "908--911",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "5",

}

TY - JOUR

T1 - Asymmetric total synthesis of (+)-danicalipin A

AU - Yoshimitsu, Takehiko

AU - Nakatani, Ryo

AU - Kobayashi, Akihiro

AU - Tanaka, Tetsuaki

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)

UR - http://www.scopus.com/inward/record.url?scp=79952154974&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=79952154974&partnerID=8YFLogxK

U2 - 10.1021/ol1029518

DO - 10.1021/ol1029518

M3 - Article

C2 - 21288044

AN - SCOPUS:79952154974

VL - 13

SP - 908

EP - 911

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 5

ER -

Asymmetric total synthesis of (+)-danicalipin A

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this