| Literature DB >> 30596506 |
Jian-Chao Deng1, Yong-Chao Gao1, Zhu Zhu1, Li Xu1, Zhao-Dong Li1, Ri-Yuan Tang1,2.
Abstract
A sulfite-promoted transformation of azoles into N-difluoromethylthioureas through N-difluoromethylation and sulfuration has been developed. In this reaction, inexpensive ethyl bromodifluoroacetate and nontoxic elemental sulfur were used as the difluoromethylation and sulfuration reagents, respectively. A variety of azoles, including benzimidazoles, imidazoles, and triazoles, performed well to afford a broad range of azole thioureas in moderate to good yields.Entities:
Year: 2018 PMID: 30596506 DOI: 10.1021/acs.orglett.8b03876
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005