96854-35-2Relevant articles and documents
Enantioselective synthesis of (+)-sedamine and (-)-allosedamine
Yadav,Reddy, M. Sridhar,Rao, P. Purushothama,Prasad
, p. 4005 - 4012 (2008/03/11)
Two different approaches to the enantioselective syntheses of (+)-sedamine and (-)-allosedamine are described, both using the Sharpless asymmetric epoxidation as the key step. Regioselective reduction of epoxides, chemoselective oxidation of alcohols, ring-closing metathesis, and nucleophilic displacements were the other key steps employed. Georg Thieme Verlag Stuttgart.
ELUCIDATION OF STEREOSPECIFITY OF A SELENIUM-CONTAINING HYDROGENASE FROM METHANOCOCCUS VANNIELLII - SYNTHESIS OF (R)- AND (S)--3,4-DIHYDRO-7-HYDROXY-1-HYDROXYETHYLQUINOLINE
Teshima, Tadashi,Nakaji, Akira,Shiba, Tetsuo,Tsai, Lin,Yamazaki, Shigeko
, p. 351 - 354 (2007/10/02)
To elucidate the stereospecifity of the selenium-containing hydrogenase from Methanococcus vannielii, (R)- and (S)--3,4-dihydro-7-hydroxy-1-hydroxyethylquinoline were syntheside as authentic samples for comparison with the compound which was deri