ULTRAVIOLET IRRADIATION OF PYRIMIDINE DERIVATIVES: III. INFLUENCE OF HYDROGEN CYANIDE ON THE PHOTOLYSIS

1959 ◽  
Vol 37 (8) ◽  
pp. 1281-1287 ◽  
Author(s):  
A. M. Moore

The presence of HCN in concentrations up to 0.05 M in aqueous, buffered solutions of uracil, uridine, and 1,3-dimethyluracil has been shown to divert the normal course of the photochemical hydration reactions of these compounds as a result of photochemically induced combination between HCN and the pyrimidine derivative. A simple calculation indicates that HCN is more efficient than water in reacting with activated uracil molecules by a factor of about 103. The possible general significance of such nucleophilic addition reactions in the photochemistry of nucleic acids is discussed.

Synlett ◽  
2014 ◽  
Vol 25 (13) ◽  
pp. 1863-1868 ◽  
Author(s):  
Fumihiko Yoshimura ◽  
Keiji Tanino ◽  
Taiki Abe

2021 ◽  
Vol 25 ◽  
Author(s):  
Pavel M. Yamanushkin ◽  
Marina Rubina ◽  
Michael Rubin

: The topic of this review is the amide-directed functionalization of strained carbocycles — specifically, unsaturated or saturated three- and four-membered rings. The following approaches are discussed: a) directed carbometallation and hydrometallation of cyclopropenes catalyzed by transition metals; b) directed metal-templated nucleophilic addition reactions; c) directed C-H functionalization, including transition metal-catalyzed C-H-activation reactions; and d) directed radical additions.


Synthesis ◽  
2008 ◽  
Vol 2008 (20) ◽  
pp. 3319-3325
Author(s):  
Margaret Brimble ◽  
Daryl Crimmins ◽  
Ivaylo Dimitrov ◽  
Patrick O’Connor ◽  
Vittorio Caprio

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