Copper‐Catalyzed One‐Pot Approach to α‐Aryl Amidines via Truce‐Smiles Rearrangement
Smiles Rearrangement
Stoichiometry
Sulfonyl
DOI:
10.1002/adsc.201800490
Publication Date:
2018-06-15T01:59:30Z
AUTHORS (4)
ABSTRACT
Abstract A copper‐catalyzed one‐pot approach to α‐aryl amidines from terminal alkynes, sulfonyl azides, and aryl sulfonamides via a Truce‐Smiles rearrangement under mild condition in good excellent yields was reported for the first time. The formation of such aryl‐ sp 3 C−C bond previously could not be directly achieved by common method. stoichiometry substrates played an important role improving desired products. In addition, two sets signals were observed 1 H NMR spectra their possible cause investigated control experiments as well. magnified image
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (41)
CITATIONS (19)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....