Progress toward the total synthesis of ciguatoxins: A convergent synthesis of the FGHIJKLM ring fragment

Hiroyuki Takakura; Makoto Sasaki; Shugo Honda; Kazuo Tachibana

doi:10.1021/ol026306n

Progress toward the total synthesis of ciguatoxins: A convergent synthesis of the FGHIJKLM ring fragment

Hiroyuki Takakura, Makoto Sasaki, Shugo Honda, Kazuo Tachibana

LIF - Molecular and Chemical Life Science

Research output: Contribution to journal › Article › peer-review

59 Citations (Scopus)

Abstract

(Matrix presented) A highly convergent synthetic route to the FGHIJKLM ring fragment of ciguatoxins has been developed, which relied on extensive use of the B-alkyl Suzuki Miyaura coupling reaction.

Original language	English
Pages (from-to)	2771-2774
Number of pages	4
Journal	Organic letters
Volume	4
Issue number	16
DOIs	https://doi.org/10.1021/ol026306n
Publication status	Published - 2002 Aug 8

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol026306n

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title = "Progress toward the total synthesis of ciguatoxins: A convergent synthesis of the FGHIJKLM ring fragment",

abstract = "(Matrix presented) A highly convergent synthetic route to the FGHIJKLM ring fragment of ciguatoxins has been developed, which relied on extensive use of the B-alkyl Suzuki Miyaura coupling reaction.",

author = "Hiroyuki Takakura and Makoto Sasaki and Shugo Honda and Kazuo Tachibana",

year = "2002",

month = aug,

day = "8",

doi = "10.1021/ol026306n",

language = "English",

volume = "4",

pages = "2771--2774",

journal = "Organic Letters",

issn = "1523-7060",

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T1 - Progress toward the total synthesis of ciguatoxins

T2 - A convergent synthesis of the FGHIJKLM ring fragment

AU - Takakura, Hiroyuki

AU - Sasaki, Makoto

AU - Honda, Shugo

AU - Tachibana, Kazuo

PY - 2002/8/8

Y1 - 2002/8/8

N2 - (Matrix presented) A highly convergent synthetic route to the FGHIJKLM ring fragment of ciguatoxins has been developed, which relied on extensive use of the B-alkyl Suzuki Miyaura coupling reaction.

AB - (Matrix presented) A highly convergent synthetic route to the FGHIJKLM ring fragment of ciguatoxins has been developed, which relied on extensive use of the B-alkyl Suzuki Miyaura coupling reaction.

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U2 - 10.1021/ol026306n

DO - 10.1021/ol026306n

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JO - Organic Letters

JF - Organic Letters

IS - 16

ER -

Progress toward the total synthesis of ciguatoxins: A convergent synthesis of the FGHIJKLM ring fragment

Abstract

ASJC Scopus subject areas

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