Synthesis of alkaloid-like compounds via the bridging Ritter reaction

Hemtasin, C; Ung, AT; Kanokmedhakul, S; Kanokmedhakul, K; Bishop, R; Satraruji, T; Bishop, D

Synthesis of alkaloid-like compounds via the bridging Ritter reaction

Hemtasin, C Ung, AT

Kanokmedhakul, S Kanokmedhakul, K Bishop, R Satraruji, T Bishop, D

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Publication Type:: Journal Article
Citation:: Monatshefte fur Chemie, 2012, 143 (6), pp. 955 - 963
Issue Date:: 2012-06-01

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Field	Value	Language
dc.contributor.author	Hemtasin, C	en_US
dc.contributor.author	Ung, AT https://orcid.org/0000-0002-5665-0702	en_US
dc.contributor.author	Kanokmedhakul, S	en_US
dc.contributor.author	Kanokmedhakul, K	en_US
dc.contributor.author	Bishop, R	en_US
dc.contributor.author	Satraruji, T	en_US
dc.contributor.author	Bishop, D https://orcid.org/0000-0002-6533-4410	en_US
dc.date.issued	2012-06-01	en_US
dc.identifier.citation	Monatshefte fur Chemie, 2012, 143 (6), pp. 955 - 963	en_US
dc.identifier.issn	0026-9247	en_US
dc.identifier.uri	http://hdl.handle.net/10453/18042
dc.description.abstract	Alkaloid-like compounds containing a benzo[c]azepine core structure were successfully prepared in three steps from 5H-dibenzo[a,d]cyclohepten-5-ol via the bridging Ritter reaction. Biological studies of these compounds revealed that some of them are AChE inhibitors and antimalarial agents. © Springer-Verlag 2012.	en_US
dc.relation.ispartof	Monatshefte fur Chemie	en_US
dc.relation.isbasedon	10.1007/s00706-012-0759-8	en_US
dc.subject.classification	General Chemistry	en_US
dc.title	Synthesis of alkaloid-like compounds via the bridging Ritter reaction	en_US
dc.type	Journal Article
utslib.citation.volume	6	en_US
utslib.citation.volume	143	en_US
utslib.for	0303 Macromolecular and Materials Chemistry	en_US
utslib.for	03 Chemical Sciences	en_US
pubs.embargo.period	Not known	en_US
pubs.organisational-group	/University of Technology Sydney
pubs.organisational-group	/University of Technology Sydney/Faculty of Science
pubs.organisational-group	/University of Technology Sydney/Faculty of Science/School of Mathematical and Physical Sciences
pubs.organisational-group	/University of Technology Sydney/Strength - CCET - Centre for Clean Energy Technology
utslib.copyright.status	closed_access
pubs.issue	6	en_US
pubs.publication-status	Published	en_US
pubs.volume	143	en_US

Abstract:

Alkaloid-like compounds containing a benzo[c]azepine core structure were successfully prepared in three steps from 5H-dibenzo[a,d]cyclohepten-5-ol via the bridging Ritter reaction. Biological studies of these compounds revealed that some of them are AChE inhibitors and antimalarial agents. © Springer-Verlag 2012.

Please use this identifier to cite or link to this item:

http://hdl.handle.net/10453/18042