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The intramolecular Stille reaction in some target natural product syntheses

Authors :
Gerald Pattenden
David J. Sinclair
Source :
Journal of Organometallic Chemistry. 653:261-268
Publication Year :
2002
Publisher :
Elsevier BV, 2002.

Abstract

A chronological summary of the contributions made by researchers in Nottingham, UK, to developing the scope for the intramolecular Stille reaction in target natural product syntheses, e.g. leinamycin, the virginiamycins, macrolactin A, rhizoxin, the amphidinolides, lophotoxin, and pateamine, is described.

Subjects

Subjects :
Natural product
Scope (project management)
Rhizoxin
Stereochemistry
Organic Chemistry
Leinamycin
Biochemistry
Stille reaction
Inorganic Chemistry
chemistry.chemical_compound
chemistry
Intramolecular force
Lophotoxin
Materials Chemistry
Organic chemistry
Physical and Theoretical Chemistry

Details

ISSN :
0022328X
Volume :
653
Database :
OpenAIRE
Journal :
Journal of Organometallic Chemistry
Accession number :
edsair.doi...........b9da2ffdf79f895608b69a03e86e6493
Full Text :
https://doi.org/10.1016/s0022-328x(02)01169-5
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