Skip to Main content Skip to Navigation
Journal articles

Mild and Metal-Free Diastereoselective Synthesis of N-tert-Butanesulfinylamines by Using Tetrakis(dimethylamino)ethylene

Abstract : A mild and metal-free diastereoselective synthesis of N-tert-butanesulfinylamines was developed by using a strategy based on tetrakis(dimethylamino)ethylene. Good yields and diastereoselectivities were achieved by addition of o-nitrobenzyl chloride or 4-[4-(chloromethyl)phenyl]-1,2-dimethyl-5-nitro-1H-imidazole to readily available N-tert-butanesulfinimines.
Document type :
Journal articles
Complete list of metadatas

https://hal-amu.archives-ouvertes.fr/hal-01425582
Contributor : Cédric Spitz <>
Submitted on : Tuesday, January 3, 2017 - 4:16:15 PM
Last modification on : Thursday, January 18, 2018 - 2:00:24 AM
Long-term archiving on: : Tuesday, April 4, 2017 - 2:39:21 PM

File

s-0034-1378636.pdf
Publisher files allowed on an open archive

Identifiers

Collections

Citation

Cédric Spitz, Anna Lin, Thierry Terme, Patrice Vanelle. Mild and Metal-Free Diastereoselective Synthesis of N-tert-Butanesulfinylamines by Using Tetrakis(dimethylamino)ethylene. SYNTHESIS, Georg Thieme Verlag, 2014, ⟨10.1055/s-0034-1378636⟩. ⟨hal-01425582⟩

Share

Metrics

Record views

200

Files downloads

244