412299-71-9Relevant articles and documents
Synthesis of isoindoles by one-electron reductions of dibenzo[1,4]diazocines
Bovenkerk, Marcel,Esser, Birgit
, p. 775 - 785 (2015/01/30)
A synthetic protocol to isoindoles is reported through one-electron reductions of dibenzo[1,4]diazocines. The utility of the approach has been demonstrated through the synthesis of six novel isoindole derivatives. Photophysical measurements revealed emissions between 440 and 460 nm. A reaction mechanism, supported by experimental results and quantum chemical calculations, is postulated.
A new strategy for deprotonative functionalization of aromatics: Transformations with excellent chemoselectivity and unique regioselectivities using t-Bu-P4 base
Imahori, Tatsushi,Kondo, Yoshinori
, p. 8082 - 8083 (2007/10/03)
A new strategy for deprotonative functionalization of aromatics using t-Bu-P4 base has been developed, and highly chemoselective transformations have been achieved with unique regioselectivities. Copyright