Skip to Main content Skip to Navigation
Journal articles

TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion

Aïda R. Nadji-Boukrouche 1, 2, 3 Omar Khoumeri 1 Thierry Terme 1 Messaoud Liacha 3 Patrice Vanelle 1
1 ICR - Institut de Chimie Radicalaire
2 Département de Génie des Procédés
3 Laboratoire de Synthèse et de Biocatalyse Organique (LSBO)
Abstract : We describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-benzoxazolones by the reaction of aromatic carbonyl and α-carbonyl ester derivatives with a benzoxazolinonic anion formed exclusively via the TDAE strategy.
Keywords : METHODOLOGY RING ALDEHYDES LIGANDS 2(3H)-BENZOXAZOLONE benzylic alcohols oxiranes ORIGINAL SYNTHESIS DERIVATIVES benzoxazolinonic anion benzoxazolone TDAE
Document type :
Journal articles
Complete list of metadatas

Cited literature [35 references]  Display  Hide  Download
https://hal-amu.archives-ouvertes.fr/hal-01234886
Contributor : Administrateur Hal Amu <>
Submitted on : Tuesday, December 1, 2015 - 4:35:09 PM
Last modification on : Wednesday, December 12, 2018 - 2:52:05 PM
Long-term archiving on: : Wednesday, March 2, 2016 - 10:40:12 AM

File

Vignette du document
molecules-20-01262.pdf
Publisher files allowed on an open archive

Identifiers

Collections

UNIV-AMU | CNRS | INC-CNRS

Citation

Aïda R. Nadji-Boukrouche, Omar Khoumeri, Thierry Terme, Messaoud Liacha, Patrice Vanelle. TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion. Molecules, MDPI, 2015, 20, pp.1262-1276. ⟨10.3390/molecules20011262⟩. ⟨hal-01234886⟩

Export

BibTeX TEI DC DCterms EndNote

Share

Metrics

Record views

169

Files downloads

333