Reactions of alkyl (halomethyl)furancarboxylates with hexamethylenetetramine. Lapina, I., Pevzner, L., & Potekhin, A. Russian Journal of General Chemistry, 76(8):1304-1309, 2006. cited By 2
Paper doi abstract bibtex All isomers of (aminomethyl)furancarboxylic acids were prepared by the Delepine reaction from alkyl (halomethyl)furancarboxylates. Treatment of the initially formed quaternary salt with an ethanolic HCl solution yielded the salts of the corresponding unstable amino acid esters. A procedure for their purification to a high degree of purity was developed. Hydrolysis of the crude esters yielded stable amino acid salts. © Nauka/Interperiodica 2006.
@ARTICLE{Lapina20061304,
author={Lapina, I.M. and Pevzner, L.M. and Potekhin, A.A.},
title={Reactions of alkyl (halomethyl)furancarboxylates with hexamethylenetetramine},
journal={Russian Journal of General Chemistry},
year={2006},
volume={76},
number={8},
pages={1304-1309},
doi={10.1134/S1070363206080251},
note={cited By 2},
url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-33749394412&doi=10.1134%2fS1070363206080251&partnerID=40&md5=595d8dd3026456a14ef45b6191d3be98},
affiliation={St. Petersburg State University, Universitetskii pr. 26, St. Petersburg, 198504, Russian Federation},
abstract={All isomers of (aminomethyl)furancarboxylic acids were prepared by the Delepine reaction from alkyl (halomethyl)furancarboxylates. Treatment of the initially formed quaternary salt with an ethanolic HCl solution yielded the salts of the corresponding unstable amino acid esters. A procedure for their purification to a high degree of purity was developed. Hydrolysis of the crude esters yielded stable amino acid salts. © Nauka/Interperiodica 2006.},
correspondence_address1={Lapina, I.M.; St. Petersburg State University, Universitetskii pr. 26, St. Petersburg, 198504, Russian Federation},
issn={10703632},
language={English},
abbrev_source_title={Russ. J. Gen. Chem.},
document_type={Article},
source={Scopus},
}
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