Journal article

Diastereocontrolled synthesis of hydroxylated lactams

Abstract:: Highly diastereoselective reductions and organometallic additions in bicyclic lactams have been observed, which appear to result either from a stereoelectronic interaction of the pyramidalised nitrogen lone pair or from steric interactions in the bicyclic system. These products can be readily deprotected to give hydroxylated lactams.

Publication status:: Published

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APA Style

Andrews, M. D., Brewster, A., & Moloney, M. (2002). Diastereocontrolled synthesis of hydroxylated lactams. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2(1), 80–90.

MLA Style

Andrews, MD, et al. “Diastereocontrolled Synthesis of Hydroxylated Lactams.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, vol. 2, no. 1, 2002, pp. 80–90.

Chicago Style

Andrews, MD, A Brewster, and M Moloney. 2002. “Diastereocontrolled Synthesis of Hydroxylated Lactams.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 2 (1): 80–90.
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Publisher copy:: 10.1039/b108056n

Authors

+ Andrews, MD More by this author

Role:: Author

+ Brewster, A More by this author

Role:: Author

+ Moloney, M More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

Journal:: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 More from this journal
Volume:: 2
Issue:: 1
Pages:: 80-90
Publication date:: 2002-01-01
DOI:: 10.1039/b108056n
EISSN:: 1364-5463
ISSN:: 1472-7781

Language:: English
Pubs id:: pubs:38024
UUID:: uuid:ea036957-ab5f-42e6-b3c4-315d6b5e566a
Local pid:: pubs:38024
Source identifiers:: 38024
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_ea036957ab5f42e6b3c4315d6b5e566a

Terms of use

Copyright date:: 2002

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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