scholarly journals Intramolecular Hydrogen Abstraction Reaction Promoted by N-Radicals in Carbohydrates. Synthesis of Chiral 7-Oxa-2-azabicyclo[2.2.1]heptane and 8-Oxa-6-azabicyclo[3.2.1.]octane Ring Systems.

ChemInform ◽  
2003 ◽  
Vol 34 (25) ◽  
Author(s):  
Cosme G. Francisco ◽  
Antonio J. Herrera ◽  
Ernesto Suarez
1985 ◽  
Vol 14 (1) ◽  
pp. 15-18 ◽  
Author(s):  
Yoshifumi Tanimoto ◽  
Masanobu Takashima ◽  
Megumu Uehara ◽  
Michiya Itoh ◽  
Mitsuo Hiramatsu ◽  
...  

1975 ◽  
Vol 28 (12) ◽  
pp. 2629 ◽  
Author(s):  
J Stals ◽  
MG Pitt

VESCF(BJ)CI MO reactivity indices were used to provide a consistent rationale for the ground state structure, thermal decomposition and chemistry of nitroguanidine (1). Intra- and inter-molecular NH...O and NH...N hydrogen bonds, attractive and repulsive coulombic forces between nitrogen and oxygen atoms, appear to determine the crystal structure of (1). An intramolecular hydrogen-abstraction reaction and the cleavage of the molecule's weakest bond, viz. (H2N)2C-NNO2, appear to be the main primary thermal decomposition pathways for (1). The nitrimino nitrogen atom and the carbon atom were postulated to be the centres of electrophilic and nucleophilic substitution reactions respectively.


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