N-Acyltrifluoromethanesulfonamides as new chemoselective acylating agents for aliphatic and aromatic amines
-
Add time:07/13/2019 Source:sciencedirect.com
This work describes advances in the study of the internal condensation of ammonium salts of N-acylsulfonamides. N-Acyltrifluoromethanesulfonamides show considerable advantages over the non fluorinated analogues by virtue of their higher reactivity and acidity. The reaction chemoselectivity has been investigated using a wide range of amines. The sensitivity of the reaction to steric and electronic effects confirms the potential application of these reagents in chemoselective acylation of polyamines.
We also recommend Trading Suppliers and Manufacturers of N-(3-methylphenyl)-3-(4-{[(1-phenylethyl)amino]sulfonyl}phenyl)propanamide (cas 723243-61-6). Pls Click Website Link as below: cas 723243-61-6 suppliers
Prev:Bioactivity of a series of substituted N(3-phenyl-2-propenylidene)benzeneamines: a microcalorimetric study
Next:Regioselective synthesis and through-space 13C–19F spin–spin coupling NMR of new tetracyclic 3-(trifluoromethyl)-spiro(chromen[4,3-c]pyrazole-4,1′-cycloalkanes)) - 【Back】【Close 】【Print】【Add to favorite 】


