TY - JOUR
T1 - Thioamidation via Sulfur-Promoted Coupling of N-Methyliminodiacetyl Acylborons and Amines
AU - Yang, Hao
AU - Liao, Yanyan
AU - Jiang, Xuefeng
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2026/1/9
Y1 - 2026/1/9
N2 - Thioamides were efficiently synthesized via a one-pot, chemoselective coupling of MIDA acylboronates, amines, and inorganic sulfur sources. The key step in this transformation involved the condensation of MIDA acylboronates with amines to generate an imine intermediate, which subsequently underwent nucleophilic addition with sulfur species. The nucleophilicity of linear polysulfides promoted S–S bond cleavage, followed by a concerted elimination to furnish the thioamides. A variety of sensitive functional groups, including unprotected hydroxyl, carboxyl, and alkynyl substitution moieties, are well tolerated under the reaction conditions. The formation of dipeptides and the late-stage incorporation of thioamide motifs further highlight the utility of this method.
AB - Thioamides were efficiently synthesized via a one-pot, chemoselective coupling of MIDA acylboronates, amines, and inorganic sulfur sources. The key step in this transformation involved the condensation of MIDA acylboronates with amines to generate an imine intermediate, which subsequently underwent nucleophilic addition with sulfur species. The nucleophilicity of linear polysulfides promoted S–S bond cleavage, followed by a concerted elimination to furnish the thioamides. A variety of sensitive functional groups, including unprotected hydroxyl, carboxyl, and alkynyl substitution moieties, are well tolerated under the reaction conditions. The formation of dipeptides and the late-stage incorporation of thioamide motifs further highlight the utility of this method.
UR - https://www.scopus.com/pages/publications/105027230682
U2 - 10.1021/acs.joc.5c02513
DO - 10.1021/acs.joc.5c02513
M3 - 文章
AN - SCOPUS:105027230682
SN - 0022-3263
VL - 91
SP - 428
EP - 439
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 1
ER -