Stereospecific construction of substituted piperidines. Synthesis of (−)-paroxetine and (+)-laccarin
作者:John F. Bower、Thomas Riis-Johannessen、Peter Szeto、Andrew J. Whitehead、Timothy Gallagher
DOI:10.1039/b617260a
日期:——
Short and efficient enantioselective syntheses of (â)-paroxetine and (+)-laccarin are described based on the highly stereospecific cleavage of C(3)-substituted 1,3-cyclic sulfamidates.
基于对C(3)取代的1,3-环状氨基磺酸盐的高度立体选择性裂解,对(-)帕罗西汀和(+)拉卡林的短程高效对映选择性合成进行了描述。