Concise access toward chiral hydroxy phenylpropanoids: Formal synthesis of Virolongin B; Kigelin; Kurasoin A; 4-Hydroxysattabacin and Actinopolymorphol A

Patil, S.N.; Tilve, S.G.

dc.contributor.author	Patil, S.N.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2016-07-22T11:01:18Z
dc.date.available	2016-07-22T11:01:18Z
dc.date.issued	2016
dc.identifier.citation	Tetrahedron Letters. 57(30); 2016; 3371-3375.	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2016.06.070
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/4425
dc.description.abstract	A simple, two step strategy consisting of Sharpless asymmetric dihydroxylation followed by regioselective breaking of C-O bond is utilized to target key chiral intermediates of natural products virolongin B, kigelin, kurasoin A, 4-hydroxy-sattabacin and actinopolymorphol A. Derivatives of enantiopure hydroxy phenyl propanoids and ?-hydroxy Weinreb amides are synthesized. The reductive cleavage of C-O bond in a regioselectve manner is obtained using Pd/C in methanol.	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chemistry	en_US
dc.title	Concise access toward chiral hydroxy phenylpropanoids: Formal synthesis of Virolongin B; Kigelin; Kurasoin A; 4-Hydroxysattabacin and Actinopolymorphol A	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y