1,1′-Bis(thymine)ferrocene Nucleoside: Synthesis and Study of Its Stereoselective Formation

ChemPlusChem ◽  
2017 ◽  
Vol 82 (6) ◽  
pp. 859-866 ◽  
Author(s):  
Iurii Anisimov ◽  
Sebastian Saloman ◽  
Alexander Hildebrandt ◽  
Heinrich Lang ◽  
Damian Trzybiński ◽  
...  
Keyword(s):  
Nucleoside Synthesis

ChemInform Abstract: Pentenyl Ribosides: New Reagents for Purine Nucleoside Synthesis.

ChemInform ◽  
2010 ◽  
Vol 25 (16) ◽  
pp. no-no
Author(s):  
M.-C. CHAPEAU ◽  
L. J. MARNETT
Keyword(s):  
Purine Nucleoside ◽  
Nucleoside Synthesis

scholarly journals The Chemoselective Reduction of Isoxazolineγ-Lactams Through Iminium Aza-Diels-Alder Reactions: A Short-Cut Synthesis of Aminols as Valuable Intermediates towards Nucleoside Derivatives

2012 ◽  
Vol 2012 ◽  
pp. 1-10
Author(s):  
Misal Giuseppe Memeo ◽  
Mariella Mella ◽  
Paolo Quadrelli
Keyword(s):  
Catalytic Oxidation ◽  
Ring Opening ◽  
Diels Alder ◽  
Mild Conditions ◽  
Nucleoside Synthesis ◽  
Conformationally Locked

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.

3′-Deoxy-3′-hydroxymethyl-aldopentopyranosyl nucleoside synthesis. Part I

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