Syntheses of (-)-hygrine and (-)-norhygrine via Wacker oxidation

Majik, M.S.; Tilve, S.G.

dc.contributor.author	Majik, M.S.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-04T02:36:21Z
dc.date.available	2015-06-04T02:36:21Z
dc.date.issued	2010
dc.identifier.citation	Tetrahedron Letters. 51(21); 2010; 2900-2902.	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2010.03.098
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2407
dc.description.abstract	Hygrine is an important biosynthetic intermediate for tropane alkaloids. A synthesis of (-)-hygrine starting from L-proline is described. The acetonyl side chain of hygrine was fashioned through the Wittig reaction followed by regioselective Wacker oxidation. In addition, this Letter provides the first synthesis of (-)-norhygrine.	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chemistry	en_US
dc.title	Syntheses of (-)-hygrine and (-)-norhygrine via Wacker oxidation	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y