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

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