TY - JOUR
T1 - The Same Oxidation-State Introduction of Hypervalent Sulfur via Transition-Metal Catalysis
AU - Wang, Ming
AU - Jiang, Xuefeng
N1 - Publisher Copyright:
© 2021 The Chemical Society of Japan & Wiley-VCH GmbH
PY - 2021/12
Y1 - 2021/12
N2 - Sulfonyl compounds have attracted considerable interest due to their extensive applications in drug discovery, agricultural, and material science. The access to the assembly of SO2-containing compounds via the same oxidative-state introduction of hypervalent sulfur has come to the fore in the recent years. Especially, the transition-metal-involved synthesis of hypervalent sulfur compounds is the most effective strategy since SO2 is easy to insert into the metal-carbon bonds. This review discusses the application of the same oxidation-state introduction of hypervalent sulfur strategy under the transition-metal-catalyzed conditions, and presents according to different metal catalysts and the synthesized diversity hypervalent sulfur-containing compounds skeletons, including sulfonamides, sulfones, sulfinamides, sulfonyl acids and sulfonyl fluorides.
AB - Sulfonyl compounds have attracted considerable interest due to their extensive applications in drug discovery, agricultural, and material science. The access to the assembly of SO2-containing compounds via the same oxidative-state introduction of hypervalent sulfur has come to the fore in the recent years. Especially, the transition-metal-involved synthesis of hypervalent sulfur compounds is the most effective strategy since SO2 is easy to insert into the metal-carbon bonds. This review discusses the application of the same oxidation-state introduction of hypervalent sulfur strategy under the transition-metal-catalyzed conditions, and presents according to different metal catalysts and the synthesized diversity hypervalent sulfur-containing compounds skeletons, including sulfonamides, sulfones, sulfinamides, sulfonyl acids and sulfonyl fluorides.
UR - https://www.scopus.com/pages/publications/85099916964
U2 - 10.1002/tcr.202000162
DO - 10.1002/tcr.202000162
M3 - 文章
C2 - 33496372
AN - SCOPUS:85099916964
SN - 1527-8999
VL - 21
SP - 3338
EP - 3355
JO - Chemical Record
JF - Chemical Record
IS - 12
ER -