Synthesis of the H ring of gambierol

Isao Kadota; Akio Ohno; Yasuhisa Matsukawa; Yoshinori Yamamoto

doi:10.1016/S0040-4039(98)01312-4

Synthesis of the H ring of gambierol

Isao Kadota, Akio Ohno, Yasuhisa Matsukawa, Yoshinori Yamamoto

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

56 Citations (Scopus)

Abstract

Stereoselective synthesis of the H ring of gambierol was achieved from 2-deoxy-D-ribose by using the intramolecular reaction of allylstannane with aldehyde as a key step. Modified Stille coupling was successfully applied for the construction of the triene side chain.

Original language	English
Pages (from-to)	6373-6376
Number of pages	4
Journal	Tetrahedron Letters
Volume	39
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(98)01312-4
Publication status	Published - Aug 27 1998
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(98)01312-4

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title = "Synthesis of the H ring of gambierol",

abstract = "Stereoselective synthesis of the H ring of gambierol was achieved from 2-deoxy-D-ribose by using the intramolecular reaction of allylstannane with aldehyde as a key step. Modified Stille coupling was successfully applied for the construction of the triene side chain.",

author = "Isao Kadota and Akio Ohno and Yasuhisa Matsukawa and Yoshinori Yamamoto",

year = "1998",

month = aug,

day = "27",

doi = "10.1016/S0040-4039(98)01312-4",

language = "English",

volume = "39",

pages = "6373--6376",

journal = "Tetrahedron Letters",

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T1 - Synthesis of the H ring of gambierol

AU - Kadota, Isao

AU - Ohno, Akio

AU - Matsukawa, Yasuhisa

AU - Yamamoto, Yoshinori

PY - 1998/8/27

Y1 - 1998/8/27

N2 - Stereoselective synthesis of the H ring of gambierol was achieved from 2-deoxy-D-ribose by using the intramolecular reaction of allylstannane with aldehyde as a key step. Modified Stille coupling was successfully applied for the construction of the triene side chain.

AB - Stereoselective synthesis of the H ring of gambierol was achieved from 2-deoxy-D-ribose by using the intramolecular reaction of allylstannane with aldehyde as a key step. Modified Stille coupling was successfully applied for the construction of the triene side chain.

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U2 - 10.1016/S0040-4039(98)01312-4

DO - 10.1016/S0040-4039(98)01312-4

M3 - Article

AN - SCOPUS:0032572911

SN - 0040-4039

VL - 39

SP - 6373

EP - 6376

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

Synthesis of the H ring of gambierol

Abstract

ASJC Scopus subject areas

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