A Practical Aryliodine(I/III) Catalysis for the Vicinal Diamination of Styrenes
2,6-Disubstituted iodoarenes bearing amide-functionalized side arms are reported as new structures in redox-active iodine(I/III) catalysis. In combination with bis-sulfonimides as nitrogen sources and 3-chloroperbenzoic acid (mCPBA) as benign terminal oxi
Cots, Eric,Flores, Andrea,Romero, R. Martín,Mu?iz, Kilian
p. 3028 - 3031
(2019/03/26)
Oxidative diamination promoted by dinuclear iodine(III) reagents
New dinuclear iodine(III) reagents for the intermolecular diamination of alkenes are reported. These are accessible through protolytic aminolysis events, which generate defined imido-iodine(III) groups.
R?ben, Caren,Souto, José A.,Escudero-Adán, Eduardo C.,Mu?iz, Kilian
supporting information
p. 1008 - 1011
(2013/04/10)
Iodine(III)-promoted intermolecular diamination of alkenes
A rapid and productive vicinal diamination of alkenes takes place in the presence of a hypervalent iodine(III) reagent and bissulfonimides as nitrogen sources. A total of more than 60 examples are presented. The reaction is characterized by its robustness and its wide substrate scope: it proceeds selectively with both terminal and internal alkenes and tolerates a range of functional groups.
Souto, Jose A.,Gonzalez, Yolanda,Iglesias, Alvaro,Zian, Debora,Lishchynskyi, Anton,Muniz, Kilian
supporting information; experimental part
p. 1103 - 1111
(2012/07/17)
More Articles about upstream products of 1374869-29-0