Phytochemical studies on Stemona burkillii prain: Two new dihydrostemofoline alkaloids

Mungkornasawakul, P; Pyne, SG; Jatisatienr, A; Lie, W; Ung, AT; Issakul, K; Sawatwanich, A; Supyen, D; Jatisatienr, C

Phytochemical studies on Stemona burkillii prain: Two new dihydrostemofoline alkaloids

Mungkornasawakul, P Pyne, SG Jatisatienr, A Lie, W Ung, AT

Issakul, K Sawatwanich, A Supyen, D Jatisatienr, C

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Publication Type:: Journal Article
Citation:: Journal of Natural Products, 2004, 67 (10), pp. 1740 - 1743
Issue Date:: 2004-10-01

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Field	Value	Language
dc.contributor.author	Mungkornasawakul, P	en_US
dc.contributor.author	Pyne, SG	en_US
dc.contributor.author	Jatisatienr, A	en_US
dc.contributor.author	Lie, W	en_US
dc.contributor.author	Ung, AT https://orcid.org/0000-0002-5665-0702	en_US
dc.contributor.author	Issakul, K	en_US
dc.contributor.author	Sawatwanich, A	en_US
dc.contributor.author	Supyen, D	en_US
dc.contributor.author	Jatisatienr, C	en_US
dc.date.issued	2004-10-01	en_US
dc.identifier.citation	Journal of Natural Products, 2004, 67 (10), pp. 1740 - 1743	en_US
dc.identifier.issn	0163-3864	en_US
dc.identifier.uri	http://hdl.handle.net/10453/8690
dc.description.abstract	Two new dihydrostemofoline alkaloids, 11(S),12(R)-dihydrostemofoline (3) and stemoburkilline (4), along with stemofoline (1) and 2′- hydroxystemofoline (2) have been isolated from a root extract of Stemona burkillii Prain. The structure and relative configuration of 3 have been determined via spectroscopic data and from comparison with synthetic 11(S),12(S)-dihydrostemofoline (5). The configuration of the exo-cyclic alkene group in 4 is tentively assigned as E on the basis of mechanistic considerations.	en_US
dc.relation.ispartof	Journal of Natural Products	en_US
dc.relation.isbasedon	10.1021/np049791z	en_US
dc.subject.classification	Medicinal & Biomolecular Chemistry	en_US
dc.title	Phytochemical studies on Stemona burkillii prain: Two new dihydrostemofoline alkaloids	en_US
dc.type	Journal Article
utslib.citation.volume	10	en_US
utslib.citation.volume	67	en_US
utslib.for	0601 Biochemistry and Cell Biology	en_US
utslib.for	03 Chemical Sciences	en_US
utslib.for	06 Biological Sciences	en_US
utslib.for	11 Medical and Health 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	10	en_US
pubs.publication-status	Published	en_US
pubs.volume	67	en_US

Abstract:

Two new dihydrostemofoline alkaloids, 11(S),12(R)-dihydrostemofoline (3) and stemoburkilline (4), along with stemofoline (1) and 2′- hydroxystemofoline (2) have been isolated from a root extract of Stemona burkillii Prain. The structure and relative configuration of 3 have been determined via spectroscopic data and from comparison with synthetic 11(S),12(S)-dihydrostemofoline (5). The configuration of the exo-cyclic alkene group in 4 is tentively assigned as E on the basis of mechanistic considerations.

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http://hdl.handle.net/10453/8690