Journal article

Palladium-catalysed cyclisation of N-alkynyl aminomalonates.

Abstract:: Go around in (hetero)cycles! The palladium-catalysed tandem cyclisation/coupling reaction of alkynyl- and alkenyl-substituted aminomalonates leads to highly functionalised pyrrolidines and piperidines in good yield (see scheme). The reaction allows efficient access to a broad range of synthetically valuable building blocks. © 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim.

Publication status:: Published

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APA Style

Hess, W., & Burton, J. (2010). Palladium-catalysed cyclisation of N-alkynyl aminomalonates. Chemistry (Weinheim an Der Bergstrasse, Germany), 16(41), 12303–12306.

MLA Style

Hess, W, and J Burton. “Palladium-Catalysed Cyclisation of N-Alkynyl Aminomalonates.” Chemistry (Weinheim an Der Bergstrasse, Germany), vol. 16, no. 41, 2010, pp. 12303–06.

Chicago Style

Hess, W, and J Burton. 2010. “Palladium-Catalysed Cyclisation of N-Alkynyl Aminomalonates.” Chemistry (Weinheim an Der Bergstrasse, Germany) 16 (41): 12303–6.
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Publisher copy:: 10.1002/chem.201001951

Authors

+ Hess, W More by this author

Role:: Author

+ Burton, J More by this author

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

Journal:: Chemistry (Weinheim an der Bergstrasse, Germany) More from this journal
Volume:: 16
Issue:: 41
Pages:: 12303-12306
Publication date:: 2010-11-01
DOI:: 10.1002/chem.201001951
EISSN:: 1521-3765
ISSN:: 0947-6539

Language:: English
Keywords:: copper

palladium

aminomalonates

pyrrolidines

nitrogen heterocycles
Pubs id:: pubs:73314
UUID:: uuid:063d7a40-2d87-4710-9458-6196e3bb336e
Local pid:: pubs:73314
Source identifiers:: 73314
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_063d7a402d87471094586196e3bb336e

Terms of use

Copyright date:: 2010

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

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