Journal
CHEMISTRYSELECT
Volume 6, Issue 33, Pages 8839-8842Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202101676
Keywords
Bronsted Acid; N-dealkylation; N-alkyl(sulfon)amide; Primary amides
Categories
Funding
- Sichuan Science and Technology Program [2018JY0247]
- Antibiotics Research and Reevaluation Key Laboratory of Sichuan Province [ARRLKF17-04]
- Key Laboratory of Medicinal and Edible Plants Resources Development of Sichuan Education Department [10Y201708]
Ask authors/readers for more resources
A simple and efficient Bronsted-acid-promoted N-dealkylation method has been developed for N-alkylamides and N-alkylsulfonamides, offering a wide substrate scope and excellent chemical selectivity to produce primary (sulfon)amide derivatives in moderate to good yields without the need for transition-metal catalysts.
A simple and efficient Bronsted-acid-promoted N-dealkylation of N-alkylamides and N-alkylsulfonamides has been developed. This strategy features an ample substrate scope with excellent chemical selectivity, affording primary (sulfon)amide derivatives in moderate to good yields without the need for transition-metal catalysts.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
