Benzoxazoline ring substituted ketene N,O-acetals 3 were synthesized by the reaction of ketene S,S-acetals 2 with 2-aminophenol.The tautomeric equilibrium of some 3 was also observed.
Sulfated tin oxide (STO) has been found to be an efficient reusable solid superacid catalyst for C3-alkylation and O-alkylation of 4-hydroxycoumarins with benzylic, allylic alcohols/and corresponding acetates respecti...Sulfated tin oxide (STO) has been found to be an efficient reusable solid superacid catalyst for C3-alkylation and O-alkylation of 4-hydroxycoumarins with benzylic, allylic alcohols/and corresponding acetates respectively, in acetic acid under reflux conditions with good yield of products.展开更多
Chiral amines are synthetically versatile intermedi-ates used for the preparation of a wide range of biologically active compounds and drugs.Compared with the well-developed synthesis ofα-stereogenic amines,the estab...Chiral amines are synthetically versatile intermedi-ates used for the preparation of a wide range of biologically active compounds and drugs.Compared with the well-developed synthesis ofα-stereogenic amines,the establishment of enantioselective protocols to accessβ-stereogenic amines are very limited.展开更多
基金This work was supported by the National Natural Science Foundation of China
文摘Benzoxazoline ring substituted ketene N,O-acetals 3 were synthesized by the reaction of ketene S,S-acetals 2 with 2-aminophenol.The tautomeric equilibrium of some 3 was also observed.
文摘Sulfated tin oxide (STO) has been found to be an efficient reusable solid superacid catalyst for C3-alkylation and O-alkylation of 4-hydroxycoumarins with benzylic, allylic alcohols/and corresponding acetates respectively, in acetic acid under reflux conditions with good yield of products.
基金This work was supported by the Ministry of Education(MOE)of Singapore(no.R-143-000-A93-112).
文摘Chiral amines are synthetically versatile intermedi-ates used for the preparation of a wide range of biologically active compounds and drugs.Compared with the well-developed synthesis ofα-stereogenic amines,the establishment of enantioselective protocols to accessβ-stereogenic amines are very limited.