Journal article icon

Journal article

A multicomponent coupling strategy suitable for the synthesis of the triene component of the oxazolomycin antibiotics.

Abstract:

Concise and versatile routes suitable for the synthesis of three geometric isomers of an analogue of the left hand triene sub-unit of oxazolomycin are reported. A strategy based upon a key Heck reaction was unsuccessful, and this was traced to a combination of steric encumbrance and electronic deactivation of the alkene substrate. An alternative Stille coupling strategy, however, proved to be both versatile and high yielding, and is potentially applicable to the synthesis of analogues with va...

Expand abstract
Publication status:
Published

Actions


Access Document


Publisher copy:
10.1039/b306925g

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
Journal:
Organic and biomolecular chemistry More from this journal
Volume:
1
Issue:
21
Pages:
3726-3737
Publication date:
2003-11-01
DOI:
EISSN:
1477-0539
ISSN:
1477-0520
Language:
English
Keywords:
Pubs id:
pubs:32558
UUID:
uuid:59adfae6-e058-47b6-b3f5-14ebef80387e
Local pid:
pubs:32558
Source identifiers:
32558
Deposit date:
2012-12-19

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP