Journal article icon

Journal article

Carbamate-directed hydroboration: Enantioselective synthesis of the excitatory amino acid 1-aminocyclopentane-1,3-dicarboxylic acid

Abstract:
Carbamate-directed hydroboration (using BH3) of 1-substituted 3- cyclopentenes 2, 6 and 9 and an enantioselective synthesis of the excitatory amine acid 1-aminocyclopentane-1,3-dicarboxylic acid via carbamate-directed asymmetric hydroboration [90% de, 45% ee using (+)-IpcBH2] of cyclopentene 2 are described.
Publication status:
Published

Actions

Access Document

Publisher copy:
10.1016/S0040-4039(98)00490-0

Authors

More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Journal:
TETRAHEDRON LETTERS More from this journal
Volume:
39
Issue:
20
Pages:
3357-3358
Publication date:
1998-05-14
DOI:
ISSN:
0040-4039


Language:
English
Keywords:
Pubs id:
pubs:36488
UUID:
uuid:f2cbbd33-8470-40fb-af4e-c788b383c853
Local pid:
pubs:36488
Source identifiers:
36488
Deposit date:
2012-12-19
ARK identifier:

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