Total synthesis of an aglycone of spiramycin

作者: G Oddon , D Uguen

DOI: 10.1016/S0040-4039(97)10758-4

关键词:

摘要: Abstract The iodoaldehyde β- 8f has been converted efficiently into the title aglycone by means of Kishi-Nozaki-Takai coupling reaction.

参考文章(7)
Gary E. Keck, Anandan Palani, Stanton F. McHardy, Total Synthesis of (+)-Carbonolide B Journal of Organic Chemistry. ,vol. 59, pp. 3113- 3122 ,(1994) , 10.1021/JO00090A032
Kuniaki Tatsuta, Yoshiya Amemiya, Shunji Maniwa, Mitsuhiro Kinoshita, Total synthesis of carbomycin B and josamycin (leucomycin A3) Tetrahedron Letters. ,vol. 21, pp. 2837- 2840 ,(1980) , 10.1016/S0040-4039(00)78621-7
K. C. Nicolaou, M. R. Pavia, S. P. Seitz, Synthesis of 16-membered-ring macrolide antibiotics. 4. Carbomycin B and leucomycin A3: total synthesis of cyclic key intermediate Journal of the American Chemical Society. ,vol. 103, pp. 1224- 1226 ,(1981) , 10.1021/JA00395A044
Noriyuki NAKAJIMA, Kouichi UOTO, Osamu YONEMITSU, Tadashi HATA, Facile Total Synthesis of Carbonolides by Witting-Hoener Macro-Cyclization and Stereoselective Epoxidation Chemical & Pharmaceutical Bulletin. ,vol. 39, pp. 64- 74 ,(1991) , 10.1248/CPB.39.64