Metal-Free Trans-Aziridination of Zerumbone: Synthesis and Biological Evaluation of Aziridine Derivatives of Zerumbone

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DC Field	Value	Language
dc.contributor.author	Greeshma, G	-
dc.contributor.author	Dhanya, B P	-
dc.contributor.author	Saranya, J	-
dc.contributor.author	Reshmitha, T R	-
dc.contributor.author	Baiju, T V	-
dc.contributor.author	Meenu, M T	-
dc.contributor.author	Mangalam S Nair	-
dc.contributor.author	Nisha, P	-
dc.contributor.author	Radhakrishnan, K V	-
dc.date.accessioned	2017-10-23T11:51:51Z	-
dc.date.available	2017-10-23T11:51:51Z	-
dc.date.issued	2017-06-08	-
dc.identifier.citation	European Journal of Organic Chemistry, (21):3072-3077	en_US
dc.identifier.uri	http://hdl.handle.net/123456789/2950	-
dc.description.abstract	Herein, we describe a metal-free, iodosobenzene diacetate mediated trans-aziridination of zerumbone by the direct use of sulfonamides. Preliminary in vitro screening showed that the synthesized compounds had better antiproliferative and antidiabetic activities than the parent compound zerumbone.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Zerumbone	en_US
dc.subject	Hypervalent compounds	en_US
dc.subject	Nitrogen heterocycles	en_US
dc.subject	Small ring systems	en_US
dc.subject	Sulfonamides	en_US
dc.title	Metal-Free Trans-Aziridination of Zerumbone: Synthesis and Biological Evaluation of Aziridine Derivatives of Zerumbone	en_US
dc.type	Article	en_US
Appears in Collections:	2017

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