88039-26-3Relevant academic research and scientific papers
Trimethylchlorosilane-Mediated Mild α-Chlorination of 1,3-Dicarbonyl Compounds Promoted by Phenyliodonium Diacetate
Chong, Siying,Su, Yingpeng,Wu, Lili,Zhang, Weigang,Ma, Junyan,Chen, Xiaowei,Huang, Danfeng,Wang, Ke-Hu,Hu, Yulai
, p. 1359 - 1370 (2016/05/02)
Trimethylchlorosilane was used as chlorine source for the α-chlorination of 1,3-dicarbonyl compounds with phenyliodonium diacetate as oxidant at room temperature. The reaction allows the selective synthesis of α-monochlorinated products from different kinds of 1,3-dicarbonyl compounds in good yield. The potential possibility of this conversion for bromination has also been investigated.
A Useful Synthesis of 3-Halogeno-1-azabutadiene Derivatives, and Their Applicability in the Preparation of Heterocycles
Barluenga, Jose,Tomas, Miguel,Lopez-Ortiz, J. Francisco,Gotor, Vicente
, p. 2273 - 2276 (2007/10/02)
Azabutadiene derivatives (1) are halogenated in a selective manner with N-chlorosuccinimide or N-bromosuccinimide at the Cβ-enamine carbon.The resultant halogenated compounds (3) are suitable precursors for the synthesis of 2-oxopyrimidines and
