Total Synthesis of Nucleoside Antibiotics Amicetin, Plicacetin, and Cytosaminomycin A‐D

Author(s):  
Jiqiang Fu ◽  
Peng Xu ◽  
Biao Yu
Synlett ◽  
2017 ◽  
Vol 29 (04) ◽  
pp. 440-446 ◽  
Author(s):  
Christian Ducho ◽  
Daniel Wiegmann ◽  
Anatol Spork ◽  
Giuliana Niro

Naturally occurring nucleoside antibiotics (e.g., muraymycins and caprazamycins) represent attractive lead structures for the development of urgently needed novel antibacterial agents. One major challenge in the total synthesis of muraymycins, caprazamycins, and their analogues is the efficient construction of the densely functionalized aminoribosylated uridine-derived core unit. In order to avoid tedious protecting-group manipulations, we have aimed to conduct the aminoribosylation step with an acid-labile glycosyl acceptor. Therefore, different glycosylation approaches have been studied, with pentenyl glycosides giving the best results.


2018 ◽  
Vol 83 (13) ◽  
pp. 7076-7084 ◽  
Author(s):  
Jiqiang Fu ◽  
Stephane Laval ◽  
Biao Yu

1982 ◽  
Vol 23 (52) ◽  
pp. 5471-5474
Author(s):  
G Pattenden
Keyword(s):  

Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
M Ishibashi ◽  
S Hanazawa ◽  
Y Uchino ◽  
X Li ◽  
MA Arai

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