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Synthesis of alkenyl 3-hydroxy-2-naphthoates Full article

Journal Russian Journal of Physical Chemistry A
ISSN: 0036-0244 , E-ISSN: 1531-863X
Output data Year: 2016, Volume: 90, Number: 12, Pages: 2393-2396 Pages count : 4 DOI: 10.1134/s0036024416120360
Authors Zubareva N.D. 1 , Godunova L.F. 1 , Kurilov D.V. 1 , Razmanov I.V. 1 , Klabunovskii E.I. 1 , Stakheev A.Yu. 1 , Kustov L.M. 1,2
Affiliations
1 Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia
2 Department of Chemistry, Moscow State University, Moscow, Russia

Abstract: Esterification of 3-hydroxy-2-naphthoic acid with homologous primary and secondary alkenyl alcohols with different chain lengths in the presence of N,N'-carbonyldiimidazole (CDI) and 1,8-diazabicyclo[ 5.4.0]undec-7-ene (DBU) in N,N-dimethylformamide gave the corresponding esters.
Cite: Zubareva N.D. , Godunova L.F. , Kurilov D.V. , Razmanov I.V. , Klabunovskii E.I. , Stakheev A.Y. , Kustov L.M.
Synthesis of alkenyl 3-hydroxy-2-naphthoates
Russian Journal of Physical Chemistry A. 2016. V.90. N12. P.2393-2396. DOI: 10.1134/s0036024416120360 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000387416500012
≡ Scopus: 2-s2.0-85013928960
≡ OpenAlex: W2546993718
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