Stereoselective entry to 1'-C-branched 4'-thionucleosides from 4-thiofuranoid glycal: synthesis of 4'-thioangustmycin C
暂无分享,去创建一个
[1] S. Yamamura,et al. Synthesis of enantiomerically pure 9[(1′R,2′R,3′S)-bis(hydroxymethyl)thietan-1′-yl]adenine, 3′-thio analog of oxetanocin A , 1999 .
[2] R. T. Walker,et al. Stereoselective synthesis of novel 1′-substituted 2′-deoxy-4-thionucleosides , 1999 .
[3] Kazuo T. Nakamura,et al. Electrophilic addition to 4-thio furanoid glycal: a highly stereoselective entry to 2′-deoxy-4′-thio pyrimidine nucleosides , 1998 .
[4] A. Matsuda,et al. A facile, alternative synthesis of 4'-thioarabinonucleosides and their biological activities. , 1997, Journal of medicinal chemistry.
[5] B. Samuelsson,et al. Synthesis of 2',3'-Dideoxy-3'-C-(hydroxymethyl)-4'-thionucleosides as Potential Inhibitors of HIV , 1994 .
[6] T. Miyasaka,et al. Pummerer Rearrangement of Selenium-Containing Uracil Nucleosides , 1992 .
[7] R. T. Walker,et al. The synthesis and antiviral activity of some 4'-thio-2'-deoxy nucleoside analogues. , 1991, Journal of medicinal chemistry.
[8] R. Friesen,et al. Preparation of C-aryl glucals via the palladium catalyzed coupling of metalated aromatics with 1-iodo-3,4,6-tri-O-(triisopropylsilyl)-D-glucal , 1991 .
[9] J. M. Riordan,et al. Synthesis and biological activity of 2'-deoxy-4'-thio pyrimidine nucleosides. , 1991, Journal of medicinal chemistry.
[10] Y. Tohda,et al. A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines , 1975 .