103931-20-0Relevant articles and documents
Enamines as Surrogates of Alkyl Carbanions for the Direct Conversion of Secondary Amides to α-Branched Ketones
Liu, Yong-Peng,Wang, Shu-Ren,Chen, Ting-Ting,Yu, Cun-Cun,Wang, Ai-E,Huang, Pei-Qiang
supporting information, p. 971 - 975 (2019/01/25)
A direct transformation of secondary amides into α-branched ketones with enamines as soft alkylation reagents was developed. In this reaction, enamines serve as surrogates of alkyl carbanions, rather than the conventional enolates equivalents in the Stork's reactions, which allowed for the easy introduction of alkyl groups with electrophilic functional groups. In the presence of 4 ? molecular sieves, the method can be extended to the one-pot coupling of secondary amides with aldehydes to yield ketones. (Figure presented.).
Efficient synthesis of alkyl aryl ketones & ketals via palladium-catalyzed regioselective arylation of vinyl ethers
Liu, Mingcui,Hyder, Zeynab,Sun, Yawei,Tang, Weijun,Xu, Lijin,Xiao, Jianliang
supporting information; experimental part, p. 2012 - 2015 (2010/07/04)
The combination of Pd(OAc)2 with 1,3-bis(diphenylphosphino) propane (dppp) in ethylene glycol constitutes a high-performance catalytic system for highly regioselective arylation of a range of electron-rich vinyl ethers by aryl bromides to provide, upon hydrolysis, alkyl aryl ketones and cyclic ketals in good yields with up to 3.75 × 105 TON and 15625 h-1 TOF.