128727-98-0Relevant academic research and scientific papers
Arylation Using Sulfonamides: Phenylacetamide Synthesis through Tandem Acylation-Smiles Rearrangement
Barlow, Helen L.,Rabet, Pauline T. G.,Durie, Alastair,Evans, Tim,Greaney, Michael F.
, p. 9033 - 9035 (2019)
A range of electron-poor and heterocyclic sulfonamides react with phenylacetyl chlorides to produce benzhydryl derivatives in a single step. The reaction proceeds via tandem amide bond formation/Dohmori-Smiles rearrangement under the simple conditions of
STRAD-BINDING AGENTS AND USES THEREOF
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Paragraph 0793-0795, (2021/08/06)
Disclosed herein, inter alia, are compounds for binding STRAD pseudokinase and uses thereof.
REACTION OF ORGANIC AZIDES WITH UNSATURATED COMPOUNDS. X. N-ARYLSULFONYLCARBOXIMIDIC ESTERS
Semenov, V. P.,Ogloblin, K. A.
, p. 2154 - 2161 (2007/10/02)
N-Arylsulfonylcarboximidic esters were obtained in the reaction of arenesulfonyl azides with 1-methoxypropene, 2-methyl-1-methoxypropene, 1-alkoxycyclohexenes, and 3,3,5,5-tetramethyl-1-ethoxycyclohexene.Hydrolysis of the imidic esters gave N-arylsulfonyl
