Conversion of Olefins into Five-membered Nitrogen Heterocycles by Radical Cyclization

Heterocycles ◽  
1989 ◽  
Vol 28 (2) ◽  
pp. 1157 ◽  
Author(s):  
Derrick L. J. Clive ◽  
Ali Y. Mohammed
ChemInform ◽  
2005 ◽  
Vol 36 (18) ◽  
Author(s):  
Stephen P. Fletcher ◽  
Derrick L. J. Clive ◽  
Jianbiao Peng ◽  
David A. Wingert

ChemInform ◽  
2010 ◽  
Vol 26 (44) ◽  
pp. no-no
Author(s):  
W. R. BOWMAN ◽  
P. T. STEPHENSON ◽  
A. R. YOUNG

Synlett ◽  
2019 ◽  
Vol 30 (04) ◽  
pp. 464-470 ◽  
Author(s):  
Michael Luescher ◽  
Jeffrey Bode

Saturated nitrogen heterocycles can be found with increasing abundance in bioactive molecules despite a limited number of methods to access these scaffolds. However, the coupling of recently introduced SnAP [tin (Sn) amine protocol] reagents with a wide range of aldehydes and ketones has proven to be a reliable, practical, and versatile one-step approach to saturated N-heterocycles. While effective, the lack of mechanistic understanding limits efforts to develop new catalytic and enantioselective variants. To distinguish between a polar or radical mechanism, we assessed Lewis and Brønsted acids, radical trapping experiments, and radical clock SnAP reagents reinforcing the current understanding of the SnAP protocol as a radical cyclization.


2005 ◽  
Vol 7 (1) ◽  
pp. 23-26 ◽  
Author(s):  
Stephen P. Fletcher ◽  
Derrick L. J. Clive ◽  
Jianbiao Peng ◽  
David A. Wingert

2005 ◽  
Vol 83 (6-7) ◽  
pp. 543-545 ◽  
Author(s):  
Philippe Gaudreault ◽  
Christian Drouin ◽  
Jean Lessard

The first examples of intramolecular addition of primary amidyl radicals to olefins are described. Amidyl radicals were generated from N-(phenylthio)amides in refluxing benzene using a catalytic amount of 2,2′-azobis(isobutyronitrile) (5 mol%) and tributyltin hydride (~2.2 equiv.). The resulting yields of cyclic products ranged from 63% to 85%.Key words: radical cyclization, amidyl radicals, nitrogen heterocycles.


1997 ◽  
Vol 161 ◽  
pp. 179-187
Author(s):  
Clifford N. Matthews ◽  
Rose A. Pesce-Rodriguez ◽  
Shirley A. Liebman

AbstractHydrogen cyanide polymers – heterogeneous solids ranging in color from yellow to orange to brown to black – may be among the organic macromolecules most readily formed within the Solar System. The non-volatile black crust of comet Halley, for example, as well as the extensive orangebrown streaks in the atmosphere of Jupiter, might consist largely of such polymers synthesized from HCN formed by photolysis of methane and ammonia, the color observed depending on the concentration of HCN involved. Laboratory studies of these ubiquitous compounds point to the presence of polyamidine structures synthesized directly from hydrogen cyanide. These would be converted by water to polypeptides which can be further hydrolyzed to α-amino acids. Black polymers and multimers with conjugated ladder structures derived from HCN could also be formed and might well be the source of the many nitrogen heterocycles, adenine included, observed after pyrolysis. The dark brown color arising from the impacts of comet P/Shoemaker-Levy 9 on Jupiter might therefore be mainly caused by the presence of HCN polymers, whether originally present, deposited by the impactor or synthesized directly from HCN. Spectroscopic detection of these predicted macromolecules and their hydrolytic and pyrolytic by-products would strengthen significantly the hypothesis that cyanide polymerization is a preferred pathway for prebiotic and extraterrestrial chemistry.


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