1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation
Web of Science
AuthorPorubsky, M; Tenora, L; Potacek, M
AffiliationSchool of Chemistry
Document TypeJournal Article
CitationsPorubsky, M., Tenora, L. & Potacek, M. (2016). 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation. MOLECULES, 21 (2), https://doi.org/10.3390/molecules21020187.
Access StatusOpen Access
This paper describes the synthesis of precursors with a benzo[b]furan skeleton for the intramolecular 1,3-dipolar cycloaddition of azomethine ylides prepared from N-substituted 3-allyl-aminobenzo[b]furan-2-aldehydes and secondary amines derived from α-amino acid esters. Reactions were initiated by heating. The products consisted of four fused rings with three stereogenic centers. Their structure and stereochemistry were determined by NMR spectra and X-ray measurements.
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