A-new synthesis of N-sulfinylamines via β-elimination of chloroform from trichloromethanesulfinamides

Samuel Braverman, Marina Cherkinsky

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The synthesis of various N-monosubstituted trichloromethanesulfinamides by two alternative and novel procedures is described. All these compounds have been found to undergo base-induced elimination of chloroform with formation of the corresponding N-sulfinylamines. Reaction proceeds smoothly under mild conditions.

Original languageEnglish
Pages (from-to)487-490
Number of pages4
JournalTetrahedron Letters
Volume38
Issue number3
DOIs
StatePublished - 20 Jan 1997

Bibliographical note

Funding Information:
This work was supported by the French Research National Agency (ANR) through the Vulnerability Milieu and Climate program (VULSACO project, No. ANR-06-VMC-009 ) and RELIEF MICROLIT . The authors benefitted from highly constructive discussions with D. Idier, (BRGM, Orléans, France). We thank a lot ATT technical and scientific translation company for the English corrections.

Fingerprint

Dive into the research topics of 'A-new synthesis of N-sulfinylamines via β-elimination of chloroform from trichloromethanesulfinamides'. Together they form a unique fingerprint.

Cite this