Stereoselective Total Syntheses of (+)-exo- and (–)-exo-Brevicomins, (+)-endo- and (–)  -endo-Brevicomins, (+)- and (–)-Cardiobutanolides, (+)-Goniofufurone

Pal, Pinki; Shaw, A K

dc.contributor.author	Pal, Pinki
dc.contributor.author	Shaw, A K
dc.date.accessioned	2011-08-18T11:17:28Z
dc.date.available	2011-08-18T11:17:28Z
dc.date.issued	2011
dc.identifier.citation	Tetrahedron (2011), 67(22), 4036-4047	en
dc.identifier.uri	http://hdl.handle.net/123456789/711
dc.description.abstract	Stereoselective total syntheses of aggregation pheromones (+)-exo-brevicomin (9a), (–)-exo-brevicomin (9b), (+)-endo-brevicomin (9c), (–)-endo-brevicomin (9d) and styryllactones (+)-cardiobutanolide (14a), (–)-cardiobutanolide (14b) and (+)-goniofufurone (19a) were achieved in good yields from enantiomerically pure highly functionalized furanoid glycal building blocks (1a–d) involving similar synthetic strategies, thus making these furanoid glycals highly useful building blocks in diversity-oriented synthesis (DOS).	en
dc.format.extent	647139 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	cdricommunicationno.8048	en
dc.subject	Brevicomin	en
dc.subject	Chiral Building Blocks	en
dc.subject	Cardiobutanolide	en
dc.subject	Goniofufurone Vinylbutyrolactone	en
dc.title	Stereoselective Total Syntheses of (+)-exo- and (–)-exo-Brevicomins, (+)-endo- and (–) -endo-Brevicomins, (+)- and (–)-Cardiobutanolides, (+)-Goniofufurone	en
dc.type	Article	en