Facile generation of α,α-dibromodimethyl ketals from alkynes using TsNBr2
摘要:
TsNBr2 reacts with alkyne in the presence of methanol to form alpha,alpha-dibromodimethyl ketals instantaneously. The reaction proceeds smoothly at room temperature without using any other catalyst. The one step reaction can be carried out with both aromatic and aliphatic alkynes in excellent yield. (C) 2014 Elsevier Ltd. All rights reserved.
Facile generation of α,α-dibromodimethyl ketals from alkynes using TsNBr2
作者:Kamal Krishna Rajbongshi、Prodeep Phukan
DOI:10.1016/j.tetlet.2014.01.123
日期:2014.3
TsNBr2 reacts with alkyne in the presence of methanol to form alpha,alpha-dibromodimethyl ketals instantaneously. The reaction proceeds smoothly at room temperature without using any other catalyst. The one step reaction can be carried out with both aromatic and aliphatic alkynes in excellent yield. (C) 2014 Elsevier Ltd. All rights reserved.
Iron(III) catalyzed halo-functionalization of alkynes
作者:Bryant Catano、John Lee、Claudia Kim、David Farrell、Jeffrey L. Petersen、Yalan Xing
DOI:10.1016/j.tetlet.2015.05.039
日期:2015.7
Aromatic and aliphatic alkynes can be halo-functionalized to alpha,alpha-dihalodimethyl ketals catalyzed by FeCl3 in excellent yields. MeOH is used as a nucleophilic solvent and N-halosuccinimide as the halogen source for this efficient transformation. The resulting alpha,alpha-dibromodimethyl ketals can be converted to the corresponding alpha,alpha-dibromoketones by treatment with 8% FeCl3 in silica gel. (C) 2015 Elsevier Ltd. All rights reserved.