A simple method for N-acylation of adenosine and cytidine nucleosides using carboxylic acids activated In-Situ with carbonyldiimidazole
ND Sinha, P Davis, LM Schultze, K Upadhya
Index: Sinha; Sinha, Nanda D.; Davis; Davis, Peter; Schultze; Schultze, Lisa M.; Upadhya; Upadhya, Krishna Tetrahedron Letters, 1995 , vol. 36, # 51 p. 9277 - 9280
Full Text: HTML
Citation Number: 11
Abstract
Carboxylic acids are activated with 1.1′-carbonyldiimidazole in acetonitrile to form N- acylimidazoles which are then treated with per-trimethylsilyl ethers of nucleosides adenosine or cytidine at ambient temperature to generate exclusively N-acylated-Adenosine or N-acylated-Cytidine derivatives.
Related Articles:
[Tripathi, Snehlata; Misra, Krishna; Sanghvi, Yogesh S. Bioorganic and Medicinal Chemistry Letters, 2005 , vol. 15, # 22 p. 5045 - 5048]
[Schulhof, J. C.; Molko, D.; Teoule, R. Tetrahedron Letters, 1987 , vol. 28, # 1 p. 51 - 54]
[Pirrung, Michael C.; Fallon, Lara; McGall, Glenn Journal of Organic Chemistry, 1998 , vol. 63, # 2 p. 241 - 246]
[Schulhof, J. C.; Molko, D.; Teoule, R. Tetrahedron Letters, 1987 , vol. 28, # 1 p. 51 - 54]