17358-77-9Relevant academic research and scientific papers
Direct access to benzo[b]furans through palladium-catalyzed oxidative annulation of phenols and unactivated internal alkynes
Kuram, Malleswara Rao,Bhanuchandra,Sahoo, Akhila K.
supporting information, p. 4607 - 4612 (2013/05/22)
2,3-Disubstituted benzo[b]furans are prepared in one step from commercially available phenols and readily accessible unactivated internal alkynes (see scheme). This Pd-catalyzed oxidative annulation has a broad substrate scope and allows access to a wide range of benzo[b]furans. Copyright
GENERATION OF α-ACYLCARBENIUM IONS: A NOVEL UNCATTALYSED C-C BOND FORMATION AT ROOM TEMPERATURE
Kulkarni, Gururaj C.,Karmarkar, Sanjay N.,Kelkar, Shriniwas L.,Wadia, Murzban S.
, p. 5189 - 5198 (2007/10/02)
Reactions of substituted desyl chloride 1 and 5 with phenol at room temperature in benzene results in C-alkylation.The reaction is shown to proceed through a benzylic α-acylcarbenium ion.This contention is supported by (i) the failure of this reaction with haloketones 8 and 22 and (ii) the different nature of products obtained when these haloketones were allowed to react in the presence of K2CO3.
