Diazonium salts, and precisely arenediazonium o-benzenedisulfonimides, have been used for the first time as efficient electrophilic partners in gold catalyzed Heck-coupling reactions. The synthetic protocol was general, easy and gave the target products in satisfactory yields. Mechanistic insights revealed the fundamental roles of the o-benzenedisulfonimide anion as an electron transfer agent thath promotes a radical pathway that does not require the presence of photocatalysts or external oxidants

Gold catalyzed Heck-coupling of arenediazonium o-benzenedisulfonimides

Stefano Dughera;Margherita Barbero
2018-01-01

Abstract

Diazonium salts, and precisely arenediazonium o-benzenedisulfonimides, have been used for the first time as efficient electrophilic partners in gold catalyzed Heck-coupling reactions. The synthetic protocol was general, easy and gave the target products in satisfactory yields. Mechanistic insights revealed the fundamental roles of the o-benzenedisulfonimide anion as an electron transfer agent thath promotes a radical pathway that does not require the presence of photocatalysts or external oxidants
2018
16
295
301
http://pubs.rsc.org/en/content/articlelanding/2018/ob/c7ob02624b#!divAbstract
Gold, Heck coupling, diazonium salts
Stefano, Dughera; Margherita, Barbero
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1657737
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