ChemInform Abstract: C-NUCLEOSIDE SYNTHESIS. IV. SYNTHESIS OF PSEUDOURIDINES MODIFIED AT THE C-5′ POSITION

1979 ◽  
Vol 10 (9) ◽  
Author(s):  
T. SATO ◽  
M. WATANABE ◽  
R. NOYORI
Keyword(s):  
ChemInform ◽  
2010 ◽  
Vol 25 (16) ◽  
pp. no-no
Author(s):  
M.-C. CHAPEAU ◽  
L. J. MARNETT

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.


Tetrahedron ◽  
1995 ◽  
Vol 51 (18) ◽  
pp. 5381-5396 ◽  
Author(s):  
Bogdan Doboszewski ◽  
Norbert Blaton ◽  
Jef Rozenski ◽  
André De Bruyn ◽  
Piet Herdewijn
Keyword(s):  

2011 ◽  
Vol 6 (8) ◽  
pp. 2048-2054 ◽  
Author(s):  
Eun-Kyoung Bang ◽  
Jiyeon Won ◽  
Dohyun Moon ◽  
Jin Yong Lee ◽  
Byeang Hyean Kim

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