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Mn-mediated oxidative radical cyclization of 2-(azidomethyl)phenyl isocyanides with carbazate: access to quinazoline-2-carboxylates.
- Source :
-
New Journal of Chemistry . 5/7/2020, Vol. 44 Issue 17, p7001-7006. 6p. - Publication Year :
- 2020
-
Abstract
- Mn-TBHP mediated oxidative radical cyclization of 2-(azidomethyl)phenyl isocyanides using methyl carbazate has been described. This procedure is realized through a cascade radical addition and aromatization process with high atom economy to furnish various heterocyclic C2 diversified quinazoline-2-carboxylate derivatives. [ABSTRACT FROM AUTHOR]
- Subjects :
- *ISOCYANIDES
*AROMATIZATION
*ATOMS
*HETEROCYCLIC chemistry
*RADICAL anions
Subjects
Details
- Language :
- English
- ISSN :
- 11440546
- Volume :
- 44
- Issue :
- 17
- Database :
- Academic Search Index
- Journal :
- New Journal of Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 143044497
- Full Text :
- https://doi.org/10.1039/d0nj00479k