Iodinane- and Metal-Free Synthesis of N-Cyano Sulfilimines: Novel and Easy Access of NH-Sulfoximines
摘要:
The synthesis of N-cyanosulfilimines can readily be achieved by reaction of the corresponding sulfides with cyanogen amine in the presence of a base and NBS or I-2 as halogenating agents. Oxidation followed by C-N bond cleavage affords synthetically useful NH-free sulfoximines.
Anodic Dehydrogenative Cyanamidation of Thioethers: Simple and Sustainable Synthesis of
<i>N</i>
‐Cyanosulfilimines
作者:Martin Klein、Siegfried R. Waldvogel
DOI:10.1002/anie.202109033
日期:2021.10.18
A novel and very simple to perform electrochemical approach for the synthesis of several N-cyanosulfilimines in good to excellent yields was established. This method provides access to biologically relevant sulfoximines by consecutive oxidation using electro-generated periodate. This route can be easily scaled-up to gram quantities. The S,N coupling is carried out at an inexpensive carbon anode by
Metal-Free Synthesis of N-Cyano-Substituted Sulfilimines and Sulfoximines
作者:Carsten Bolm、Ankur Pandey
DOI:10.1055/s-0030-1258192
日期:2010.9
corresponding sulfides, N-cyano sulfoximines can easily be accessed under metal-free conditions via the corresponding N-cyano-substituted sulfilimines. The reaction sequence involves a sulfide imination with cyanogen amide in presence of a base and N-bromosuccinimide (NBS) followed by an m-chloroperoxybenzoic acid (MCPBA) mediated oxidation of the resulting sulfilimine intermediates. halides - metal-free