摘要
以氯化三忆基苄基铵作为相转移催化剂,用2,3,4,6-四-O-乙酰基-β-D-溴代吡喃葡萄糖和2,3,4,6-四-O-乙酰基-β-D-溴经喃半乳糖与羧酸反应,合成了相应的1-O-酰基-2,3,4,6-四-O-乙酰基-β-D-吡喃葡萄糖和半乳糖。通过解析这些化合物的HNMR和红外光谱,确证其糖甙键构型为β。该相转移催化法具有反应条件温和,后处理简单和立体选择性强等优点。
1 - 0 - acyl -2,3,4,6- tetra - 0 - acetyl - B - D - glucopyranoses and 1 - 0 - acyl -2,3,4,6- tetra - 0 - acetyl - B- D - gatactopyranoses were synthesized by reaction of 2,3,4,6 -tetra - 0 - acetyl - a - D - glucopyranosyl bromide and 2,3,4,6- tetra - O - acetyl - a - D -gatactopyranosyl bromide with carboxylic acid, using trienthy benzyl ammonium chloride as phase -transfer catalyst. The method has advantages of mild reaction conditions, easy seperation of products and high stereospecificity.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
1998年第4期324-327,共4页
Chinese Journal of Organic Chemistry
关键词
四乙酰基
吡喃半乳糖
合成
酰基
phase - transfer catalysis, trienthy benzyl ammonium chloride, 1 - O - acyl -2,3,4,6 - tetra -O - acetyl - β - D - glucopyranoses, 1 - O - acyl -2,3,4,6- tetra - O - acetyl -β- D -gatactopyranoses