Journal article

Lithiation-electrophilic substitution of N-thiopivaloylazetidine.

Abstract:: The fourth protocol: the rarely studied N-thiopivaloyl group plays a crucial role in mediating efficient α lithiation and incorporation of diverse electrophiles onto an azetidine ring; in the presence of chiral ligands, this chemistry also provides the first example of an enantioselective electrophilic substitution on a four-membered ring.

Publication status:: Published

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APA Style

Hodgson, D., & Kloesges, J. (2010). Lithiation-electrophilic substitution of N-thiopivaloylazetidine. Angewandte Chemie (International Ed. in English), 49(16), 2900–2903.

MLA Style

Hodgson, D., and J. Kloesges. “Lithiation-Electrophilic Substitution of N-Thiopivaloylazetidine.” Angewandte Chemie (International Ed. in English), vol. 49, no. 16, 2010, pp. 2900–03.

Chicago Style

Hodgson, D, and J Kloesges. 2010. “Lithiation-Electrophilic Substitution of N-Thiopivaloylazetidine.” Angewandte Chemie (International Ed. in English) 49 (16): 2900–2903.
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Publisher copy:: 10.1002/anie.201000058

Authors

+ Hodgson, D More by this author

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

+ Kloesges, J More by this author

Role:: Author

Journal:: Angewandte Chemie (International ed. in English) More from this journal
Volume:: 49
Issue:: 16
Pages:: 2900-2903
Publication date:: 2010-04-01
DOI:: 10.1002/anie.201000058
EISSN:: 1521-3773
ISSN:: 1433-7851

Language:: English
Keywords:: azetidines

synthetic methods

asymmetric synthesis

electrophilic substitution

lithiation
Pubs id:: pubs:51917
UUID:: uuid:2cc7b82f-084c-45f0-bab8-bd63f56bbd74
Local pid:: pubs:51917
Source identifiers:: 51917
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2010

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

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