TY  - JOUR
AU  - Porubsky, M
AU  - Tenora, L
AU  - Potacek, M
Y2  - 2021/02/05
Y1  - 2016/02/01
SN  - 1420-3049
UR  - http://hdl.handle.net/11343/260370
AB  - 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.
LA  - English
PB  - MDPI
T1  - 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation
DO  - 10.3390/molecules21020187
IS  - Molecules
VL  - 21
IS  - 2
L1  - /bitstream/handle/11343/260370/PMC6273826.pdf?sequence=1&isAllowed=y
ER  -