Journal article

Exploiting a novel size exclusion phenomenon for enantioselective acid/base cascade catalysis.

Abstract:: A novel size exclusion phenomenon between PS-BEMP and sterically bulky BPAs, has been discovered and exploited in a one-pot base-catalysed Michael addition/acid-catalysed enantioselective N-acyliminium cyclisation cascade, allowing the preparation of structurally complex β-carbolines with moderate to good enantiocontrol.

Publication status:: Published

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APA Style

Muratore, M., Shi, L., Pilling, A., Storer, R., & Dixon, D. (2012). Exploiting a novel size exclusion phenomenon for enantioselective acid/base cascade catalysis. Chemical Communications, 48(51), 6351–6353.

MLA Style

Muratore, M, et al. “Exploiting a Novel Size Exclusion Phenomenon for Enantioselective Acid/Base Cascade Catalysis.” Chemical Communications, vol. 48, no. 51, 2012, pp. 6351–53.

Chicago Style

Muratore, M, L Shi, A Pilling, R Storer, and D Dixon. 2012. “Exploiting a Novel Size Exclusion Phenomenon for Enantioselective Acid/Base Cascade Catalysis.” Chemical Communications 48 (51): 6351–53.
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Publisher copy:: 10.1039/c2cc32258g

Authors

+ Muratore, M More by this author

Role:: Author

+ Shi, L More by this author

Role:: Author

+ Pilling, A More by this author

Role:: Author

+ Storer, R 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
Volume:: 48
Issue:: 51
Pages:: 6351-6353
Publication date:: 2012-05-23
DOI:: 10.1039/c2cc32258g
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:332761
UUID:: uuid:08f0df8b-cfb0-47ee-90cd-34324ccbf593
Local pid:: pubs:332761
Source identifiers:: 332761
Deposit date:: 2013-11-17
ARK identifier:: ark:/29072/ora_08f0df8bcfb047ee90cd34324ccbf593

Terms of use

Copyright date:: 2012

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

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