Synthesis of sulfur containing macrocycles with sucrose scaffold

被引:2
|
作者
Gajewska, Agnieszka [1 ,2 ]
Osuch-Kwiatkowska, Anna [1 ]
Jarosz, Slawomir [1 ]
机构
[1] Polish Acad Sci, Inst Organ Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland
[2] PAS, Inst Phys Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland
关键词
Sucrose; Sulfur macrocycles; Cyclization; DERIVATIVES;
D O I
10.1016/j.carres.2019.107825
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The first synthesis of sucrose-based macrocycles containing two sulfur atoms in the ring was presented. The synthesis was initiated from known 6,6'-dideoxy-6,6'-di-chloro-1',2,3,3',4,4'-hexa-O-benzyl-sucrose in which both terminal positions (C6 and C6') were elongated by the -S-CH2-CH2-OH unit. The resulting diol was converted into dichloride and reacted further with a series of diamines which afforded the corresponding macrocyclic derivatives in high yields.
引用
收藏
页数:5
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