A stereoselective synthesis of the bacchopetiolone (1) carbocyclic core using a tandem phenolic oxidation/Diels-Alder reaction is described. [reaction: see text].
Progress toward the total synthesis of bacchopetiolone: application of a tandem aromatic oxidation/Diels-Alder reaction. Publishing Authors By Initials
Progress toward the total synthesis of bacchopetiolone: application of a tandem aromatic oxidation/Diels-Alder reaction. Journal Published:
PUBLICATION TYPE: Research Support, Non-U.S. Gov
Journal: Organic letters
VOLUME: 8
Page Numbers: 5421-4
Journal Abbreviation: Org. Lett.
ISSN: 1523-7060
DAY: 23
MONTH: Nov
YEAR: 2006
Progress toward the total synthesis of bacchopetiolone: application of a tandem aromatic oxidation/Diels-Alder reaction. Information
Number of References:
LANGUAGE: eng
NlmUniqueID: 100890393
Progress toward the total synthesis of bacchopetiolone: application of a tandem aromatic oxidation/Diels-Alder reaction. Keywords Mesh Terms:
KEYWORDS: Stereoisomerism
MESH TERMS: chemical synthesis
Chemical & Substance for Abstract: Progress toward the total synthesis of bacchopetiolone: application of a tandem aromatic oxidation/Diels-Alder reaction. Information
Substance Name: bacchopetiolone
Registry Number: 0
Grant and Affiliation Information for Progress toward the total synthesis of bacchopetiolone: application of a tandem aromatic oxidation/Diels-Alder reaction.
AFFILIATION: Department of Chemistry, Yale University, New Haven, Connecticut 06520-8107, USA.
Country: United States
AGENCY: United States NCI
GRANT: R01-CA933591
ACRONYM: CA
MEDLINETA: Org Lett
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