Application of dibutyltin oxide method to regioselective acylation and alkylation of tylosin at C-4''.
K Kiyoshima, M Sakamoto, T Ishikura, Y Fukagawa, T Yoshioka, H Naganawa, T Sawa, T Takeuchi
Index: Chem. Pharm. Bull. 37(4) , 861-5, (1989)
Full Text: HTML
Abstract
4''-O-Acyl-, 4''-O-alkyl- and 4''-deoxy-tylosin derivatives were synthesized using 2'-O-acetyl-3'',4''-O-(dibutyl-stannio)tylosin as a synthetic intermediate. The in vitro biological evaluation showed that the new derivatives were active against macrolide-resistant clinical isolates of bacteria and mycoplasmas, and that they were resistant to hepatic esterase.
Related Compounds
Related Articles:
2015-03-09
[Biomacromolecules 16(3) , 868-79, (2015)]
2011-10-21
[J. Org. Chem. 76(20) , 8223-31, (2011)]
1980-01-01
[Nucleic Acids Symp. Ser. (8) , s7-8, (1980)]
2000-01-01
[Acta Pharm. Hung. 70(3-6) , 119-30, (2000)]
1995-11-22
[Carbohydr. Res. 277(2) , 231-44, (1995)]