Iodine-mediated oxythiolation of o-vinylanilides with disulfides for the synthesis of benzoxazines. Issue 12 (4th March 2022)

• Record Type: Journal Article
• Authors: Yang, Yu; Liu, Liyan; Li, Kuiliang; Zha, Zhenggen; Sun, Qi; Wang, Zhiyong
• Is Part Of: RSC advances. Volume 12:Issue 12(2022)
• Page Start: 7347
• Page End: 7351
• Publication Date: 2022-03-04
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d2ra01078j
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : An efficient iodine-mediated oxythiolation of o -vinylanilides with disulfides was developed. The reaction features high yields, is metal-free, and has a wide substrate scope. Abstract : An efficient iodine-mediated oxythiolation of o -vinylanilides with disulfides was developed. By virtue of this method, a series of thio-tethered benzoxazine derivatives were synthesized in good to excellent yields. The reaction features high yields, is metal-free, and has a wide substrate scope.