99142-96-8Relevant academic research and scientific papers
Synthesis of 2-Acyl-3,4-dihydronaphthalenes by Silver-Promoted Oxidative C-C σ-Bond Acylation/Arylation of Alkylidenecyclopropanes with α-Ketoacids
Liu, Yu,Chen, Zan,Wang, Qiao-Lin,Zhou, Cong-Shan,Xiong, Bi-Quan,Yang, Chang-An,Tang, Ke-Wen
, p. 9984 - 9994 (2019)
A novel and efficient AgNO3-facilitated oxidative C-C σ-bond difunctionalization of alkylidenecyclopropanes with α-ketoacids for preparing 2-acyl-substituted 3,4-dihydronaphthalenes is developed. This radical acylation/arylation transformation
Production method of 2-acyl-3,4-dihydronaphthalen derivatives
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Paragraph 0026; 0029; 0055; 0056, (2019/11/28)
The invention discloses a novel production method of 2-acyl-3,4-dihydronaphthalen derivatives. According to the method, methylenecyclopropane compounds and alpha-keto acid compounds are used as reaction raw materials, a reaction is carried out in a cheap
Polarized Ketene Dithioacetals. Part 42. Studies on the Reactions of Alkyl and Aryl Grignard Reagents with α-Oxoketene Dithioacetals
Singh, Gurdeep,Purkayastha, Makhan L.,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar
, p. 1289 - 1294 (2007/10/02)
The oxoketene dithioacetals (2a-k) derived from a variety of cyclic and acyclic active methylene ketones undergo 1,2-addition with methylmagnesium iodide to give the alcohol acetals (3a-k) which, on subsequent boron trifluoride-ether catalysed methanolysi
