Desymmetrization of meso-Bicyclic Hydrazines: An Efficient Strategy Towards the Synthesis of Functionalized Cyclopentenes

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DC Field	Value	Language
dc.contributor.author	Sajisha, V S	-
dc.contributor.author	Anas, S	-
dc.contributor.author	Jubi John	-
dc.contributor.author	Radhakrishnan, K V	-
dc.date.accessioned	2016-12-13T09:34:35Z	-
dc.date.available	2016-12-13T09:34:35Z	-
dc.date.issued	2009	-
dc.identifier.citation	Synlett, (18):2885-2895	en_US
dc.identifier.uri	http://hdl.handle.net/123456789/2557	-
dc.description.abstract	Desymmetrization of meso-bicyclic hydrazines offers a facile entry into the class of functionalized cyclopentenes. Various methodologies used along this direction are described in this account. Our attempts in this area proved that the palladium-catalyzed desymmetrization of these substrates with various organometallic reagents results in the formation of 3,4-disubstituted cyclopentenes.	en_US
dc.language.iso	en	en_US
dc.publisher	Thieme	en_US
dc.subject	meso-bicyclic hydrazines	en_US
dc.subject	cyclopentenes	en_US
dc.subject	palladium	en_US
dc.subject	homogenous catalysis	en_US
dc.title	Desymmetrization of meso-Bicyclic Hydrazines: An Efficient Strategy Towards the Synthesis of Functionalized Cyclopentenes	en_US
dc.type	Article	en_US
Appears in Collections:	2009

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