| Literature DB >> 30714367 |
Yanhui Guo1, Guodong Wang1, Li Wei1, Jie-Ping Wan1.
Abstract
The cascade reactions between NH2-functionalized enaminones and sulfonyl hydrazines have been developed for the synthesis of fully substituted pyrazoles. By making use of the hydrophilic primary amino group in the enaminones, the reactions proceed well in the medium of pure water in the presence of molecular iodine, TBHP, and NaHCO3 via cascade C-H sulfonylation and pyrazole annulation. The cleavage of the C-N bond in enaminones is confirmed by the experiment using 15 N-labeled enaminone.Entities:
Year: 2019 PMID: 30714367 DOI: 10.1021/acs.joc.8b02897
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354