CATALYTIC DESYMMETRIZATION OF DIAZABICYCLIC OLEFINS: A HIGHLY STEREOSELECTIVE STRATEGY TOWARDS FUNCTIONALIZED CYCLOPENTANOIDS

dc.contributor.author	Radhakrishnan, K V
dc.contributor.author	Jubi John
dc.contributor.author	Rani Rajan
dc.contributor.author	Nayana Joseph
dc.date.accessioned	2016-12-22T08:34:47Z
dc.date.available	2016-12-22T08:34:47Z
dc.date.issued	2010-12
dc.identifier.citation	Med Chem Res19:S42–S44	en_US
dc.identifier.uri	http://hdl.handle.net/123456789/2594
dc.description.abstract	One of the most important goals in contemporary synthetic organic chemistry is the development of stereoselective carbon–carbon coupling reactions providing a broadly applicable method to synthesize complex structures from simple precursors. Skeletal rearrangements of such simple precursors are powerful processes for generating molecular diversity with atom economy. In this context, desymmetrization of meso compounds provides an efficient route to asymmetric synthons of high value in a limited number of steps	en_US
dc.language.iso	en	en_US
dc.publisher	spinger science	en_US
dc.subject	coupling reactions	en_US
dc.subject	synthesize complex	en_US
dc.subject	asymmetric	en_US
dc.title	CATALYTIC DESYMMETRIZATION OF DIAZABICYCLIC OLEFINS: A HIGHLY STEREOSELECTIVE STRATEGY TOWARDS FUNCTIONALIZED CYCLOPENTANOIDS	en_US
dc.type	Article	en_US