论文信息 - Selective Deprotection of Fully Benzoylated Nucleoside Derivatives - 字舞流文

Selective Deprotection of Fully Benzoylated Nucleoside Derivatives

Abstract Selective deprotection of benzoylated hydroxyl groups is one of the crucial problems in the synthesis of nucleoside analogues as well as of other polyfunctional molecules.

P. Krausz | Vincent Roy | R. Zerrouki | A. Hadj-Bouazza

[1] M. Rahman,et al. Partial protection of carbohydrate derivatives. part 18. simple, preparative procedure for 5'-o-acylribonucleosides; highly regioselective o-deacylation at 2' and 3' positions of fully acylated purine and pyrimidine ribonucleoside through sodium methoxide-thf system , 1985 .

[2] S. Hanessian,et al. The Preparation and Synthetic Utility of tert-Butyldiphenylsilyl Ethers , 1975 .

[3] E. Corey,et al. Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives , 1972 .

[4] A. Holý. Nucleic acid components and their analogues. CLIII. Preparation of 2'-deoxy-L-ribonucleosides of the pyrimidine series , 1972 .