946570-87-2Relevant academic research and scientific papers
Synthesis of substituted 5-(pyrrolidin-2-yl)tetrazoles and their application in the asymmetric Biginelli reaction
Wu, Yong-Yong,Chai, Zhuo,Liu, Xin-Yuan,Zhao, Gang,Wang, Shao-Wu
experimental part, p. 904 - 911 (2009/07/19)
A series of chiral substituted 5-(pyrrolidin-2-yl)tetrazoles have been synthesized and evaluated as organocatalysts for the asymmetric Biginelli reaction. The relationship between catalytic activity and the different catalyst structures is briefly discussed. By using the optimized catalyst C10 (10 mol-%), a series of 3,4-dihydropyrimidin-2(1H)-one (DHPM) derivatives have been obtained in 63-88% yields and 68-81 % ee values within 24 h at room temperature.
Tetrazolic acid functionalized dihydroindol: Rational design of a highly selective cyclopropanation organocatalyst
Hartikka, Antti,Arvidsson, Per I.
, p. 5874 - 5877 (2008/02/09)
(Chemical Equation Presented) Herein we wish to report our development of an improved catalyst (S)-(-)-indoline-2-yl-1H-tetrazole (1) for the enantioselective organocatalyzed cyclopropanation of α,β-unsaturated aldehydes with sulfur ylides. The new organo
