Expanding the Scope of the Acyl-Type Radical Addition Reactions Promoted by SmI2

2006 ◽  
Vol 71 (21) ◽  
pp. 8219-8226 ◽  
Author(s):  
Jakob Karaffa ◽  
Karl B. Lindsay ◽  
Troels Skrydstrup
Keyword(s):  
Radical Addition ◽  
Addition Reactions ◽  
Type Radical

scholarly journals Expanding the Scope of the Acyl-Type Radical Addition Reactions Promoted by SmI2.

ChemInform ◽  
2007 ◽  
Vol 38 (8) ◽  
Author(s):  
Jakob Karaffa ◽  
Karl B. Lindsay ◽  
Troels Skrydstrup
Keyword(s):  
Radical Addition ◽  
Addition Reactions ◽  
Type Radical

Free radical addition reactions—IV

Tetrahedron ◽  
1965 ◽  
Vol 21 (10) ◽  
pp. 2743-2747 ◽  
Author(s):  
H. Goldwhite ◽  
M.S. Gibson ◽  
C. Harris
Keyword(s):  
Free Radical ◽  
Radical Addition ◽  
Addition Reactions ◽  
Free Radical Addition

ChemInform Abstract: CAPTODATIVE SUBSTITUENT EFFECTS. 18. KINETIC EFFECTS IN RADICAL ADDITION REACTIONS TO RADICOPHILES

1985 ◽  
Vol 16 (2) ◽  
Author(s):  
F. LAHOUSSE ◽  
R. MERENYI ◽  
J. R. DESMURS ◽  
H. ALLAIME ◽  
A. BORGHESE ◽  
...  
Keyword(s):  
Substituent Effects ◽  
Radical Addition ◽  
Addition Reactions ◽  
Kinetic Effects

N-Chloroamines as substrates for metal-free photochemical atom-transfer radical addition reactions in continuous flow

2021 ◽  
Author(s):  
Alexander Steiner ◽  
Oscar de Frutos ◽  
Juan A. Rincón ◽  
Carlos Mateos ◽  
Jason Williams ◽  
...  
Keyword(s):  
Continuous Flow ◽  
Radical Addition ◽  
Addition Reactions ◽  
Atom Transfer ◽  
Metal Free ◽  
Atom Transfer Radical Addition

N-Chloroamines have recently seen interest as substrates for atom-transfer radical addition (ATRA) reactions with olefins, to form β-chloroamine products, with complete atom incorporation. We report the development of a fully...

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