1430102-67-2Relevant academic research and scientific papers
Synthesis of Polysubstituted Pyrroles via Silver-Catalyzed Oxidative Radical Addition of Cyclopropanols to Imines
Zhou, Yulu,Wu, Mingchang,Liu, Yi,Cheng, Cungui,Zhu, Gangguo
, p. 7542 - 7546 (2020)
A silver-catalyzed formal [3 + 2] cycloaddition reaction, with cyclopropanols as a C3 subunit and imines as a two-atom subunit, is developed. The reaction takes place under mild conditions and produces a broad array of polysubstituted pyrroles in medium t
Preparation method of polysubstituted pyrrole compound
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Paragraph 0025-0029; 0030-0033, (2019/07/04)
The invention discloses a preparation method of a polysubstituted pyrrole compound. The preparation method comprises the following steps: mixing imine shown as a formula II, cyclopropanol shown as a formula III, a catalyst, an oxidant and a solvent to for
Copper-catalyzed decarboxylative coupling of alkynyl carboxylates with 1,1-dibromo-1-alkenes
Huang, Zheng,Shang, Rui,Zhang, Zi-Rong,Tan, Xiao-Dan,Xiao, Xiao,Fu, Yao
, p. 4551 - 4557 (2013/06/05)
A copper-catalyzed decarboxylative coupling reaction of potassium alkynyl carboxylates with 1,1-dibromo-1-alkenes was developed for the synthesis of unsymmetrical 1,3-diyne and 1,3,5-triyne derivatives. Diverse aryl, alkenyl, alkynyl, and alkyl substituted 1,1-dibromo-1-alkenes can react smoothly with aryl and alkyl substituted propiolates to produce unsymmetrical 1,3-diynes and 1,3,5-triynes with high selectivity and good functional group compatibility.
