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A laterally-fused N-heterocyclic carbene framework from polysubstituted aminoimidazo[5,1- b ]oxazol-6-ium salts.

Authors :
Gillie AD
Wakeling MG
Greene BL
Male L
Davies PW
Source :
Beilstein journal of organic chemistry [Beilstein J Org Chem] 2024 Mar 18; Vol. 20, pp. 621-627. Date of Electronic Publication: 2024 Mar 18 (Print Publication: 2024).
Publication Year :
2024

Abstract

A polysubstituted 3-aminoimidazo[5,1- b ]oxazol-6-ium framework has been accessed from a new nitrenoid reagent by a two-step ynamide annulation and imidazolium ring-formation sequence. Metalation with Au(I), Cu(I) and Ir(I) at the C2 position provides an L-shaped NHC ligand scaffold that has been validated in gold-catalysed alkyne hydration and arylative cyclisation reactions.<br /> (Copyright © 2024, Gillie et al.)

Details

Language :
English
ISSN :
1860-5397
Volume :
20
Database :
MEDLINE
Journal :
Beilstein journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
38533470
Full Text :
https://doi.org/10.3762/bjoc.20.54