Regioselective O2′, O3′??Deacetylations of Peracetylated Ribonucleosides by Using Tetra??n??butylammonium Fluoride
A Babu Kumar, R Manetsch
Index: Babu Kumar, Arun; Manetsch, Roman European Journal of Organic Chemistry, 2014 , vol. 2014, # 17 p. 3551 - 3555
Full Text: HTML
Citation Number: 1
Abstract
Abstract A robust, mild, and highly regioselective deacetylation of 1, 2-diol diacetates in the presence of other acetate functions was achieved by using tetra-n-butylammonium fluoride. This method provided a single-step route to access O5′-acetyl ribonucleosides, a key intermediate in the synthesis of biomedically important nucleosides and nucleotides. Moreover, it offered the general applicability of a non-enzymatic method for the selective ...
Related Articles:
[Ciuffreda, Pierangela; Casati, Silvana; Santaniello, Enzo Tetrahedron, 2000 , vol. 56, # 20 p. 3239 - 3243]
[Ciuffreda, Pierangela; Casati, Silvana; Santaniello, Enzo Tetrahedron, 2000 , vol. 56, # 20 p. 3239 - 3243]
[Nowak, Ireneusz; Jones, Carl T.; Robins, Morris J. Journal of Organic Chemistry, 2006 , vol. 71, # 8 p. 3077 - 3081]
Removal of silyl protecting groups from hydroxyl functions with ammonium fluoride in methanol
[Zhang, Weijian; Robins, Morris J. Tetrahedron Letters, 1992 , vol. 33, # 9 p. 1177 - 1180]
[Koole, Leo H.; Buck, Henk M.; Kanters, Jan A.; Schouten, Arie Canadian Journal of Chemistry, 1987 , vol. 65, p. 326 - 331]