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Protecting group free enantiospecific total syntheses of structurally diverse natural products of the tetrahydrocannabinoid family.
A simple, highly diastereoselective, Lewis acid catalyzed Friedel-Crafts coupling of a cyclic allylic alcohol with resorcinol derivatives has been developed and achieved with high atom economy, in a protecting group free manner and in less than 6 steps, the longest linear sequence. Expand
In-situ intestinal absorption and pharmacokinetic investigations of carvedilol loaded supersaturated self-emulsifying drug system.
The results conclusively confirmed that the SEDDS formulation could be considered as a new alternative delivery vehicle for the oral supply of CD. Expand