Stereoselective preparation of a key intermediate toward the synthesis of nelfinavir
A stereoselective synthesis of an intermediate that can be elaborated into the potent HTV-protease inhibitor, nelfinavir, is described. The key step of the reaction sequence is the stereoselective preparation of a bromosulfonamide from an olefin using the
Raghavan, Sadagopan,Kumar, Ch. Naveen
experimental part
p. 821 - 828
(2011/08/09)
A stereoselective synthesis of the hexahydroazepine core of (-)-balanol
A stereoselective synthesis of the hexahydroazepine core of (-)-balanol is described. The key step of the route includes the bromosulfonamidation of an olefin using the intramolecular sulfilimine group as the nucleophile and the Pummerer ene reaction.
Raghavan, Sadagopan,Kumar, Ch. Naveen
p. 1585 - 1588
(2007/10/03)
More Articles about upstream products of 783322-43-0