Stereoselective Total Synthesis of (+/-)-Nimbidiol
The first total synthesis of (+/-)-nimbidiol (1), a biogenetically interesting diterpene isolated from the root bark of Azadirachta indica Linn., has been realized through the diether (8b) prepared by a simple acid-catalyzed cyclialkylation route.
Banik, Bimal K.,Ghosh, Sukumar,Ghatak, U. R.
p. 103 - 104
(2007/10/02)
AN EFFICIENT SYNTHESIS OF 2-SUBSTITUTED 3,3-DIMETHYLCYCLOHEXAN-1-ONES. A SIMPLE SYNTHETIC ROUTE TO PODOCARPA-8,11,13-TRIENE INTERMEDIATES.
2-Substituted 3,3-dimethylcyclohexan-1-ones are conveniently prepared from the respective 2-substituted 3-methylcyclohex-2-en-1-ones through boron trifluoride-ether-mediated conjugate addition of a methyl group with lithium dimethylcuprate and those incorporating 2β-phenylethyl substituents have been further transformed to podocarpa-8,11,13-triene intermediates in excellent yields.
Banik, Bimal K.,Chakraborti, Asit K.,Ghatak, Usha Ranjan
p. 3391 - 3397
(2007/10/02)
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