A synthesis of 2-epi-amphidinolide E (1) has been accomplished via an unexpected and highly diastereoselective C(2) stereochemical inversion during the modified Yamaguchi esterification of alcohol 4b and Fe(CO)3-complexed dienoic acid 7. [reaction: see text].
Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction. Publishing Authors By Initials
Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction. Journal Published:
PUBLICATION TYPE: Research Support, N.I.H., Extr
Journal: Organic letters
VOLUME: 9
Page Numbers: 307-10
Journal Abbreviation: Org. Lett.
ISSN: 1523-7060
DAY: 18
MONTH: Jan
YEAR: 2007
Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction. Information
Number of References:
LANGUAGE: eng
NlmUniqueID: 100890393
Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction. Keywords Mesh Terms:
KEYWORDS: Stereoisomerism
MESH TERMS: chemistry
Chemical & Substance for Abstract: Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction. Information
Substance Name: amphidinolide E
Registry Number: 0
Grant and Affiliation Information for Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction.
AFFILIATION: Departments of Chemistry and Biochemistry, Scripps Florida, Jupiter, Florida 33458, USA.
Country: United States
AGENCY: United States NIGMS
GRANT: GM 38436
ACRONYM: GM
MEDLINETA: Org Lett
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