Novel conformationally locked nucleosides and oligonucleotides based on bicyclo[3.2.1]octane scaffold as a pseudosugar moiety

Author(s):  
Michal Šála ◽  
Milan Dejmek ◽  
Eliška Procházková ◽  
Hubert Hřebabecký ◽  
Jiří Rybáček ◽  
...  
2005 ◽  
Vol 15 (3) ◽  
pp. 545-550 ◽  
Author(s):  
Antonio Procopio ◽  
Stefano Alcaro ◽  
Antonio De Nino ◽  
Loredana Maiuolo ◽  
Francesco Ortuso ◽  
...  

Tetrahedron ◽  
1999 ◽  
Vol 55 (25) ◽  
pp. 7707-7724 ◽  
Author(s):  
Guangyi Wang ◽  
Jean-Luc Girardet ◽  
Esmir Gunic

2021 ◽  
Vol 47 (3) ◽  
pp. 784-787
Author(s):  
A. M. Bogdanov ◽  
D. A. Gorbachev ◽  
E. R. Zaitseva ◽  
A. Yu. Smirnov ◽  
N. S. Baleeva ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-10
Author(s):  
Misal Giuseppe Memeo ◽  
Mariella Mella ◽  
Paolo Quadrelli

Isoxazolineγ-lactams are prepared starting from the regioisomeric cycloadducts of benzonitrile oxide to theN-alkyl 2-azanorbornenes taking advantage of the efficient catalytic oxidation by RuO4. The reduction of the amide groups is easily conducted in the presence of LiAlH4under mild conditions, which allowed for the chemoselective reduction of the amide moiety followed by ring opening to afford the desired conformationally locked isoxazoline-carbocyclic aminols, as valuable intermediates for nucleoside synthesis.


1999 ◽  
Vol 40 (35) ◽  
pp. 6465-6468 ◽  
Author(s):  
Satoshi Obika ◽  
Jun-ichi Andoh ◽  
Tomomi Sugimoto ◽  
Kazuyuki Miyashita ◽  
Takeshi Imanishi

2012 ◽  
Vol 48 (91) ◽  
pp. 11214 ◽  
Author(s):  
Kabir Abdu ◽  
Miren K. Aiertza ◽  
Oliver J. Wilkinson ◽  
Jane A. Grasby ◽  
Pattama Senthong ◽  
...  

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