132316-96-2Relevant articles and documents
Enantiocontrolled synthesis of two amino acids; (S)-glutamic acid and (S)-2-aminoadipic acid
Takano,Kamikubo,Moriya,Ogasawara
, p. 601 - 604 (2007/10/02)
An efficient enantiocontrolled route to two acidic amino acids, (S)-glutamic acid and (S)-2-aminoadipic acid, has been developed starting from chiral equivalents of cyclopentadienone and cyclohexadienone, respectively.
A Synthesis of (-)-Slaframine and (-)-1,8a-Diepislaframine
Pearson, William H.,Bergmeier, Stephen C.
, p. 1976 - 1978 (2007/10/02)
Reductive cyclization of the optically pure azido epoxides 12 and 13 afforded the indolizidines 14 and 16, which were converted into (-)-slaframine 1 and (-)-1,8a-diepislaframine 18.
