Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin.

Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin. Research Abstract Details 

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Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin. Abstract Text:

Ricardo Lira,William R Roush,

[reaction: see text] A stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin has been accomplished via a highly diastereoselective double allylboration reaction of 6-8 and an iodonium ion promoted urethane cyclization for the installation of the C(15) alkoxy function in 3.

Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin. Publishing Authors By Initials

R Lira,WR Roush,

For similar organic chemicals: carboxylic acids: acids, acyclic: carbamates: urethane research abstracts see: organic chemicals: carboxylic acids: acids, acyclic: carbamates: urethane research

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Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin. Journal Published:

PUBLICATION TYPE: Research Support, N.I.H., Extr

Journal: Organic letters

VOLUME: 9

Page Numbers: 533-6

Journal Abbreviation: Org. Lett.

ISSN: 1523-7060

DAY: 1

MONTH: Feb

YEAR: 2007

Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin. Information

Number of References:

LANGUAGE: eng

NlmUniqueID: 100890393

Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin. Keywords Mesh Terms:

KEYWORDS: Urethane

MESH TERMS: chemistry

Chemical & Substance for Abstract: Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin. Information

Substance Name: Iodine

Registry Number: 7553-56-2

Grant and Affiliation Information for Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin.

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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