A general route to the synthesis of N-protected 1-substituted and   1,2-disubstituted taurines

CORC > 北京大学 > 化学与分子工程学院

	A general route to the synthesis of N-protected 1-substituted and 1,2-disubstituted taurines
	Xu, JX ; Xu, S
刊名	synthesis stuttgart
	2004
关键词	amino acid aminoalkanesulfonic acid epoxide olefin synthesis TRANSITION-STATE ISOSTERE SOLID-PHASE SYNTHESIS ASYMMETRIC-SYNTHESIS UNNATURAL BIOPOLYMERS MITSUNOBU REACTION VICINAL DIAMINES ACIDS SULFINAMIDE SULFONOPEPTIDES CONVERSION
DOI	10.1055/s-2003-44382
英文摘要	N-Benzyloxycarbonyl protected alpha-substituted and alpha,beta-disubstituted taurines were synthesized from olefins and epoxides via N-benzyloxycarbonylamino alcohol thioacetates as key intermediates. They are important sulfur analogues of naturally occurring amino acids and building blocks for the synthesis of alpha-substituted and alpha,beta-disubstituted beta-sulfonopeptides.; Chemistry, Organic; SCI(E); EI; 27; ARTICLE; 2; 276-282
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/313324]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Xu, JX,Xu, S. A general route to the synthesis of N-protected 1-substituted and 1,2-disubstituted taurines[J]. synthesis stuttgart,2004.
APA	Xu, JX,&Xu, S.(2004).A general route to the synthesis of N-protected 1-substituted and 1,2-disubstituted taurines.synthesis stuttgart.
MLA	Xu, JX,et al."A general route to the synthesis of N-protected 1-substituted and 1,2-disubstituted taurines".synthesis stuttgart (2004).