The inside cover picture, provided by Francesco Fini et al., shows a catalytic cycle, in which an in situ generated bis(2,6-diisopropyl acenaphthenequinonediimine palladium catalyst is able to divergently convert terminal and internal alkynes into propiolic esters or maleic esters and their derivatives, respectively, with a wide range of alcohols, under oxidative alkoxycarbonylation conditions (4 bar of carbon monoxide, in the presence of benzoquinone as oxidant at 20 8C). More details can be found in the full paper on pages 3244–3253 (M. Beltrani, C. Carfagna, B. Milani, R. Mancuso, B. Gabriele, F. Fini, Adv. Synth. Catal. 2016, 358, 3244–3253; DOI 10.1002/ adsc.201600521).
INSIDE COVER PICTURE
MANCUSO R;GABRIELE, Bartolo;
2016-01-01
Abstract
The inside cover picture, provided by Francesco Fini et al., shows a catalytic cycle, in which an in situ generated bis(2,6-diisopropyl acenaphthenequinonediimine palladium catalyst is able to divergently convert terminal and internal alkynes into propiolic esters or maleic esters and their derivatives, respectively, with a wide range of alcohols, under oxidative alkoxycarbonylation conditions (4 bar of carbon monoxide, in the presence of benzoquinone as oxidant at 20 8C). More details can be found in the full paper on pages 3244–3253 (M. Beltrani, C. Carfagna, B. Milani, R. Mancuso, B. Gabriele, F. Fini, Adv. Synth. Catal. 2016, 358, 3244–3253; DOI 10.1002/ adsc.201600521).I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
