Journal article

Site isolated base and acid catalyzed azaspirocyclization cascades.

Abstract:: A one-pot, site isolated base (PS-BEMP) and acid (Si-TsOH) catalyzed cyclization cascade to azaspirocyclic molecules is reported; the reaction is simple to perform, atom efficient (water is the only byproduct) and broad in its scope to a diverse range of azaspirocyclic products.

Publication status:: Published

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APA Style

Pilling, A., Böhmer, J., & Dixon, D. (2008). Site isolated base and acid catalyzed azaspirocyclization cascades. Chemical Communications, 7, 832–834.

MLA Style

Pilling, A., et al. “Site Isolated Base and Acid Catalyzed Azaspirocyclization Cascades.” Chemical Communications, no. 7, 2008, pp. 832–34.

Chicago Style

Pilling, A, J Böhmer, and D Dixon. 2008. “Site Isolated Base and Acid Catalyzed Azaspirocyclization Cascades.” Chemical Communications, no. 7: 832–34.
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Publisher copy:: 10.1039/b716568d

Authors

+ Pilling, A More by this author

Role:: Author

+ Böhmer, J More by this author

Role:: Author

+ Dixon, D More by this author

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

Journal:: Chemical Communications More from this journal
Issue:: 7
Pages:: 832-834
Publication date:: 2008-02-01
DOI:: 10.1039/b716568d
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:34119
UUID:: uuid:249c76ab-31e0-4674-a7ea-c1e227a1fe6c
Local pid:: pubs:34119
Source identifiers:: 34119
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2008

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

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