Asymmetric synthesis of double bond isomers of the structure proposed for pyrinodemin A and indication of its structural revision.
Asymmetric synthesis of double bond isomers of the structure proposed for pyrinodemin A and indication of its structural revision. Research Abstract Details
Asymmetric synthesis of double bond isomers (+)-2 (delta(15',16')) and (+)-3 (delta(14',15')) of the structure (1) (delta(16',17')) proposed for pyrinodemin A, a cytotoxic bis-pyridine alkaloid with a unique cis-cyclopent[c]isoxazolidine moiety from a marine sponge, has been accomplished. Pyrinodemin A was indicated to be a 1:1 racemic mixture of 2 from comparison of C(18 )and chiral HPLC analysis for pyrinodemin A and the synthetic compounds as well as ESIMS data of oxidative degradation products of pyrinodemin A.
Asymmetric synthesis of double bond isomers of the structure proposed for pyrinodemin A and indication of its structural revision. Publishing Authors By Initials
Asymmetric synthesis of double bond isomers of the structure proposed for pyrinodemin A and indication of its structural revision. Journal Published:
PUBLICATION TYPE: Research Support, Non-U.S. Gov
Journal: Molecules (Basel, Switzerland)
VOLUME: 10
Page Numbers: 312-6
Journal Abbreviation:
ISSN: 1420-3049
DAY: 31
MONTH: 01
YEAR: 2005
Asymmetric synthesis of double bond isomers of the structure proposed for pyrinodemin A and indication of its structural revision. Information
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LANGUAGE: eng
NlmUniqueID: 100964009
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Grant and Affiliation Information for Asymmetric synthesis of double bond isomers of the structure proposed for pyrinodemin A and indication of its structural revision.
AFFILIATION: Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
Country: Switzerland
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MEDLINETA: Molecules
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