| 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, roč. 21, č. 2, s. "nestrankovano", 11 s. ISSN 1420-3049. doi:10.3390/molecules21020187. 2016. |
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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, roč.~21, č.~2, s.~''nestrankovano'', 11 s. ISSN~1420-3049. doi:10.3390/molecules21020187. 2016.
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