129958-21-0Relevant articles and documents
Direct Transformation of Terminal Alkynes into Amidines by a Silver-Catalyzed Four-Component Reaction
Liu, Binbin,Ning, Yongquan,Virelli, Matteo,Zanoni, Giuseppe,Anderson, Edward A.,Bi, Xihe
, p. 1593 - 1598 (2019)
An unprecedented conversion of terminal alkynes into N-sulfonimidamides (amidines) is reported by a silver-catalyzed, one-pot, four-component reaction with TMSN3, sodium sulfinate, and sulfonyl azide. The reaction scope includes both aromatic and aliphatic alkynes. A possible cascade reaction mechanism, consisting of alkyne hydroazidation, sulfonyl radical addition, 1,3-dipolar cycloaddition by TMSN3, and retro-1,3-dipolar cycloaddition, is proposed. TMSN3 is found to play an essential role in each step of the reaction.
REACTION OF ORGANIC AZIDES WITH UNSATURATED COMPOUNDS XII. N-ARYLSULFONYLAMIDINES
Semenov, V. P.,Ogloblin, K. A.
, p. 716 - 719 (2007/10/02)
The reaction of ammonia, diethylamine, and piperidine with N-arylsulfonylcarboximidic esters or directly with the reaction mixtures obtained from arenesulfonyl azides and vinyl ethers gave the corresponding N-arylsulfonylamidines.