Relative β-elimination rates of heteroatoms from alkyl and aminyl radicals

1998 ◽  
pp. 1143-1144 ◽  
Author(s):  
Sunggak Kim
Keyword(s):  
Aminyl Radicals

5-Exoversus 6-EndoCyclization of Primary Aminyl Radicals:  An Experimental and Theoretical Investigation

2007 ◽  
Vol 72 (26) ◽  
pp. 10231-10234 ◽  
Author(s):  
Feng Liu ◽  
Kun Liu ◽  
Xinting Yuan ◽  
Chaozhong Li
Keyword(s):  
Theoretical Investigation ◽  
Aminyl Radicals

Probing the diastereoselectivity in the cyclization of cationic aminyl radicals

1999 ◽  
Vol 10 (21) ◽  
pp. 4091-4094 ◽  
Author(s):  
Martin Hemmerling ◽  
Åsa Sjöholm ◽  
Peter Somfai
Keyword(s):  
Aminyl Radicals

Kinetics of intramolecular additions of the aminyl radicals to carbonyl groups and subsequent ring opening

Tetrahedron ◽  
1995 ◽  
Vol 51 (31) ◽  
pp. 8437-8446 ◽  
Author(s):  
Sunggak Kim ◽  
Kwang Sub Yoon ◽  
Sung Soo Kim ◽  
Hyo Seok Seo
Keyword(s):  
Ring Opening ◽  
Carbonyl Groups ◽  
Aminyl Radicals ◽  
Kinetics Of

ChemInform Abstract: Probing the Diastereoselectivity in the Cyclization of Cationic Aminyl Radicals.

ChemInform ◽  
2010 ◽  
Vol 31 (7) ◽  
pp. no-no
Author(s):  
Martin Hemmerling ◽  
Aasa Sjoeholm ◽  
Peter Somfai
Keyword(s):  
Aminyl Radicals

A Perturbation Molecular Orbital Study of the Recombination Reactions of Diarylaminyl Radicals

1973 ◽  
Vol 28 (12) ◽  
pp. 1892-1896 ◽  
Author(s):  
Muthana Shanshal
Keyword(s):  
High Temperature ◽  
Low Temperature ◽  
Molecular Orbital ◽  
Dissociation Energy ◽  
Mo Calculations ◽  
Aminyl Radicals ◽  
Molecular Orbital Study ◽  
Aminyl Radical ◽  
High Temperature Reactions ◽  
Recombination Reactions

The recombination reactions of arylaminyl radicals are studied on the basis of its order P\10 treatment, assuming dimeric intermediates with C-N or C-C bonding modes. In the case of diphenyl aminyl radical the N -N recombination causes an increase in the T-bonding energy and should be most favourable for the low temperature reactions. Due to the low dissociation energy of the N-N bond, the C-N bonding is preferred in the high temperature reactions. It is found that the ortho- and para-additions are energetically more favourable than the meta addition, in agreement with π-SCF MO calculations and experimental results. The recombination of 2,2′-dinaphthyl aminyl radicals proceeds through C-C and C -N bonding, the 1,1′-bonding is most favourable. The PMO-results are parallel to those of the π-SCF MO calculations, providing another demonstration for the utility of this method.

ChemInform Abstract: Cyclization of Aminyl Radicals Derived from Amino Acids.

ChemInform ◽  
2010 ◽  
Vol 28 (48) ◽  
pp. no-no
Author(s):  
W. R. BOWMAN ◽  
M. J. BROADHURST ◽  
D. R. COGHLAN ◽  
K. A. LEWIS
Keyword(s):  
Amino Acids ◽  
Aminyl Radicals
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