Journal article icon

Journal article

Total synthesis of (-)-nakadomarin A.

Abstract:

A short and highly stereoselective synthesis of (-)-nakadomarin A has been developed using combinations of catalyst-controlled bond formations, one-pot multistep procedures, and powerful route-shortening reaction cascades. Several unprecedented chemical transformations were developed, including a highly Z-selective, eight-membered-ring-forming intramolecular Julia-Kocienski reaction, a highly diastereoselective intramolecular furan/iminium ion cyclization, and a sulfonic acid-controlled Z-sel...

Expand abstract
Publication status:
Published

Actions


Access Document


Publisher copy:
10.1021/ja908399s

Authors


More by this author
Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Role:
Author
Journal:
Journal of the American Chemical Society
Volume:
131
Issue:
46
Pages:
16632-16633
Publication date:
2009-11-05
DOI:
EISSN:
1520-5126
ISSN:
0002-7863
URN:
uuid:a0675fd1-11dc-4f18-b682-8a5993110826
Source identifiers:
34955
Local pid:
pubs:34955

Terms of use


Metrics


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