Synthesis of various macrosphelides by oxidative derivatization of the macrosphelide core

Yuji Matsuya; Takanori Kawaguchi; Hideo Nemoto

doi:10.3987/com-03-s26

Synthesis of various macrosphelides by oxidative derivatization of the macrosphelide core

Yuji Matsuya, Takanori Kawaguchi, Hideo Nemoto^*

^*Corresponding author for this work

Synthetic and Medicinal Chemistry

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

13 Scopus citations

Abstract

The macrosphelide core (4), simple 16-membered trilactone, was subjected to several oxidative conditions to produce various natural macrosphelide analogues, including macrosphelides A and C. This approach provided a new access to diverse macrosphelides for a study on their structure-activity relationships.

Original language	English
Pages (from-to)	39-43
Number of pages	5
Journal	Heterocycles
Volume	61
DOIs	https://doi.org/10.3987/com-03-s26
State	Published - 2003/12/31

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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@article{417776d34d1744f0b636b52547592128,

title = "Synthesis of various macrosphelides by oxidative derivatization of the macrosphelide core",

abstract = "The macrosphelide core (4), simple 16-membered trilactone, was subjected to several oxidative conditions to produce various natural macrosphelide analogues, including macrosphelides A and C. This approach provided a new access to diverse macrosphelides for a study on their structure-activity relationships.",

author = "Yuji Matsuya and Takanori Kawaguchi and Hideo Nemoto",

year = "2003",

month = dec,

day = "31",

doi = "10.3987/com-03-s26",

language = "英語",

volume = "61",

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journal = "Heterocycles",

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publisher = "Japan Institute of Heterocyclic Chemistry",

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T1 - Synthesis of various macrosphelides by oxidative derivatization of the macrosphelide core

AU - Matsuya, Yuji

AU - Kawaguchi, Takanori

AU - Nemoto, Hideo

PY - 2003/12/31

Y1 - 2003/12/31

N2 - The macrosphelide core (4), simple 16-membered trilactone, was subjected to several oxidative conditions to produce various natural macrosphelide analogues, including macrosphelides A and C. This approach provided a new access to diverse macrosphelides for a study on their structure-activity relationships.

AB - The macrosphelide core (4), simple 16-membered trilactone, was subjected to several oxidative conditions to produce various natural macrosphelide analogues, including macrosphelides A and C. This approach provided a new access to diverse macrosphelides for a study on their structure-activity relationships.

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U2 - 10.3987/com-03-s26

DO - 10.3987/com-03-s26

M3 - 学術論文

AN - SCOPUS:0346623759

SN - 0385-5414

VL - 61

SP - 39

EP - 43

JO - Heterocycles

JF - Heterocycles

ER -

Synthesis of various macrosphelides by oxidative derivatization of the macrosphelide core

Abstract

ASJC Scopus subject areas

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