87221-63-4Relevant academic research and scientific papers
Molecular Design by Cycloaddition Reaction. Part 43. Cycloaddition Reactions of Silyl Enol Ethers of 2-Acetylfuran and -thiophene and Related Benzo Analogues
Sasaki, Tadashi,Ishibashi, Yukio,Ohno, Masatomi
, p. 1972 - 1997 (2007/10/02)
The title compounds (5, 6, 11, 12 and 13) underwent cycloaddition reactions with typical dienophiles followed by oxidative rearomatization.The reactions of (5) and (6) with heterodienophiles gave rather open-chain adducts via a zwitterionic interm
UNEQUIVOCAL SYNTHESIS OF PHENACYLIDENEANILINE FROM SILYL ENOL ETHERS AND NITROSOBENZENE AND ONE-POT CYCLOADDITION REACTIONS OF THE RELATED ANILS
Sasaki, Tadashi,Ishibashi, Yukio,Ohno, Masatomi
, p. 863 - 866 (2007/10/02)
Phenacylideneaniline was formed by Et3N-catalyzed elimination reaction of the hydroxylamine obtained from silyl enol ether 5a and nitrosobenzene (6).By this method, one-pot procedure was possible for cycloaddition reactions of the related anils.From these
