|
|Section2= |Section7= |Section8= }} :''This article is about a compound used in synthesis of certain stimulants and should not be confused with a stimulant in that class the brand name of which is propalin'' Prolinol is a chiral amino-alcohol that is used as a chiral building block in organic synthesis. It exists as two enantiomers: the D and L forms. ==Preparation== Prolinol is obtained by reduction of the amino acid proline using lithium aluminium hydride.〔Dickman, D. A.; Meyers, A. I.; Smith, G. A.; Gawley, R. E. (Reduction of α-Amino Acids: L-Valinol ) Organic Syntheses, Collected Volume 7, p.530 (1990).〕〔Enders D.; Fey P.; Kipphardt, H. () Organic Syntheses, Collected Volume 8, p.26 (1993).〕 Because proline is cheaply available in high optical purity, enantiomerically pure prolinol is also widely available. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「prolinol」の詳細全文を読む スポンサード リンク
|