196795-70-7Relevant academic research and scientific papers
Cycloaddition of new N-unsubstituted azomethine ylides generated from N-(trimethylsilylmethyl)thioureas to electron-deficient olefins, acetylenes and aldehydes, synthetic equivalents of nonstabilized aminonitrile ylides
Tsuge, Otohiko,Hatta, Taizo,Tashiro, Hideki,Kakura, Yoshikazu,Maeda, Hironori,Kakehi, Akikazu
, p. 7723 - 7735 (2007/10/03)
The S-methylation of N-(trimethylsilylmethyl)thioureas and the subsequent desilylation of the silylmethyl group generates N-unsubstituted azomethine ylides having both methylthio and amino groups at the ylide carbon. These azomethine ylides undergo succes
A new and general route to N-unsubstituted azomethine ylides from N-(silylmethyl)thioureas: Cycloaddition of synthetic equivalents of nonstabilized aminonitrile ylides
Tsuge, Otohiko,Hatta, Taizo,Kakura, Yoshikazu,Tashiro, Hideki,Maeda, Hironori,Kakehi, Akikazu
, p. 945 - 946 (2007/10/03)
The S-methylation of N-(silylmethyl)thioureas followed by the desilylation generates N-unsubstituted azomethine ylides having both methylthio and amino groups at the ylide carbon. These azomethine ylides react with electron-deficient olefins to give forma
