The metathesis reaction for side chain construction in carbocyclic sinefungin analogue synthesis

被引:8
|
作者
Chen, Qi [1 ]
Liu, Chong [1 ]
Shulyak, Tetyana S. [1 ]
Schneller, Stewart W. [1 ]
机构
[1] Auburn Univ, Dept Chem & Biochem, Molette Lab Drug Discovery, Auburn, AL 36849 USA
关键词
AdoMet analogues; Carbocyclic purine nucleosides; Sinefungin; Grubbs catalysis; Metathesis; S-ADENOSYLMETHIONINE; ANTIVIRAL ACTIVITY; DRUG-TARGET; METHYLTRANSFERASE; METHYLATION; INHIBITORS; 5'-HOMOARISTEROMYCIN; SYNTHASE; VIRUSES;
D O I
10.1016/j.tet.2013.12.030
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The naturally occurring nucleoside sinefungin has found considerable use in biological investigations. More extensive sinefungin studies have been limited because few analogues have been reported due to the synthetic challenges associated with such studies. Reported herein are preparative ways to two carbocyclic sinefungin analogues: 6'-deaminocarbocyclic sinefungin and (S)-6'-hydroxy-6'-deamino-carbocyclic sinefimgin. The synthetic routes were made efficient and practical by the application of two metathesis reactions employing second generation Grubbs catalyst. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:892 / 900
页数:9
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