FACILE REDUCTIVE DEAMINATION OF ARYLAMINES USING A NEW ARENESULFONYL NITRITE

Authors
SHIN HH PARK YJ KIM YH
Citation
Hh. Shin et al., FACILE REDUCTIVE DEAMINATION OF ARYLAMINES USING A NEW ARENESULFONYL NITRITE, Heteroatom chemistry, 4(2-3), 1993, pp. 259-262
Citations number
11
Categorie Soggetti
Chemistry
Journal title
Heteroatom chemistry → ACNP
ISSN journal
10427163
Volume
4
Issue
2-3
Year of publication
1993
Pages
259 - 262
Database
ISI
SICI code
1042-7163(1993)4:2-3<259:FRDOAU>2.0.ZU;2-3
Abstract
Arenesulfonic acids were found to react with dinitrogen tetraoxide at -40-degrees-C in tetrahydrofuran to form arenesulfonyl nitrites which showed excellent diazotizing ability for the reductive deaminations of arylamines to arenes in the presence of anhydrous copper(II) halides as catalysts.