PORUBSKÝ, Martin, Lukáš TENORA a Milan POTÁČEK. 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation. Molecules. Mayer und Muller, 2016, roč. 21, č. 2, s. "nestrankovano", 11 s. ISSN 1420-3049. Dostupné z: https://dx.doi.org/10.3390/molecules21020187. |
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@article{1334127, author = {Porubský, Martin and Tenora, Lukáš and Potáček, Milan}, article_number = {2}, doi = {http://dx.doi.org/10.3390/molecules21020187}, keywords = {1 3 dipolar cycloaddition; fused heterocycles; thermal initiation; 3 aminobenzo[b]furan 2 carbaldehyde}, language = {eng}, issn = {1420-3049}, journal = {Molecules}, title = {1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation}, volume = {21}, year = {2016} }
TY - JOUR ID - 1334127 AU - Porubský, Martin - Tenora, Lukáš - Potáček, Milan PY - 2016 TI - 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation JF - Molecules VL - 21 IS - 2 SP - "nestrankovano" EP - "nestrankovano" PB - Mayer und Muller SN - 14203049 KW - 1 3 dipolar cycloaddition KW - fused heterocycles KW - thermal initiation KW - 3 aminobenzo[b]furan 2 carbaldehyde N2 - 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 alfa-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. ER -
PORUBSKÝ, Martin, Lukáš TENORA a Milan POTÁČEK. 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation. \textit{Molecules}. Mayer und Muller, 2016, roč.~21, č.~2, s.~''nestrankovano'', 11 s. ISSN~1420-3049. Dostupné z: https://dx.doi.org/10.3390/molecules21020187.
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