A convenient synthesis of 4(5)-(2-hydroxyaroyl)-5(4)-trifluoromethyl-1,2,3-triazoles from 2-trifluoromethylchromones and chromen-4-imines
摘要:
The reactions of 2-trifluoromethylchromones and 2-trifluoromethyl-4H-chromen-4-inlines with sodium azide in the presence of acetic acid give the ketone and imine derivatives of 5(4)-trifluoromethyl-1,2,3-triazole in high yields.
Electrophilic nitration of 2-trifluoromethylchromone and its 6- and 7-methoxy derivatives affords 6-, 5-, and 8-nitro derivatives, respectively, while 5,7-dimethyl-2-trifluoromethylchromone yields a 6,8-dinitro derivative. Radical chlorination results in 3-chloro derivatives.
One-pot synthesis of functionalized benzo[c]coumarins and their precursors via the reaction of 2-(polyfluoroalkyl)chromones with 4-alkyl-3-cyanocoumarins
作者:Vyacheslav Ya. Sosnovskikh、Vladislav Yu. Korotaev、Igor B. Kutyashev、Alexey Yu. Barkov、Alexander V. Safrygin
DOI:10.1039/c6ra12492e
日期:——
dichloromethane in the presence of triethylamine to give a wide variety of functionalized benzo[c]coumarin derivatives in good yields. This new annulation reaction presumably proceeds by a tandem intermolecular Michael addition and subsequent intramolecular condensationbetween an intermediate enolate anion and cyano group. In the case of 3-cyano-4-methylcoumarin and 2-(trifluoromethyl)chromones activated
2-(多氟烷基)色酮与4-烷基-3-氰基香豆素在二氯甲烷中,在三乙胺的存在下反应,以高收率得到各种官能化的苯并[ c ]香豆素衍生物。这种新的环化反应大概是通过串联分子间迈克尔加成反应以及随后的中间烯醇式阴离子和氰基之间的分子内缩合而进行的。在3-氰基-4-甲基香豆素和2-(三氟甲基)色酮被两个吸电子取代基激活的情况下,分离出三个无环中间体,并提出了可能的反应机理。
One-Pot Domino Synthesis of Polyfunctionalized Benzophenones, Dihydroxanthones, and<i>m</i>-Terphenyls from 2-(Polyfluoroalkyl)chromones
作者:Vyacheslav Ya. Sosnovskikh、Vladislav Yu. Korotaev、Alexey Yu. Barkov、Igor B. Kutyashev、Alexander V. Safrygin
DOI:10.1002/ejoc.201403585
日期:2015.3
Whereas 2-(polyfluoroalkyl)chromones activated by electron-withdrawing substituents in the benzene ring react with 2-(1-phenylalkylidene)malononitriles in the presence of triethylamine in dichloromethane to produce a wide range of polyfunctionalizedbenzophenones and dihydroxanthones, their reactions with ethyl α-cyano-β-methylcinnamate under the same conditions took an entirely different course and
Electrophilic nitration of 2-trifluoromethylchromone and its 6- and 7-methoxy derivatives affords 6-, 5-, and 8-nitro derivatives, respectively, while 5,7-dimethyl-2-trifluoromethylchromone yields a 6,8-dinitro derivative. Radical chlorination results in 3-chloro derivatives.
A convenient synthesis of 4(5)-(2-hydroxyaroyl)-5(4)-trifluoromethyl-1,2,3-triazoles from 2-trifluoromethylchromones and chromen-4-imines
作者:Vyacheslav Ya. Sosnovskikh、Boris I. Usachev
DOI:10.1070/mc2002v012n02abeh001562
日期:——
The reactions of 2-trifluoromethylchromones and 2-trifluoromethyl-4H-chromen-4-inlines with sodium azide in the presence of acetic acid give the ketone and imine derivatives of 5(4)-trifluoromethyl-1,2,3-triazole in high yields.
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作者:V. Ya. Sosnovskikh、B. I. Usachev、M. I. Kodess
DOI:10.1023/a:1021340132279
日期:——
The nitration of 5,7-dimethyl-2-polyhaloalkylchromones affords either 5,7-dimethyl-6-nitro- or 5,7-dimethyl-6,8-dinitro-2-polyhaloalkylchromones, depending on the reaction conditions. Signals in the H-1 and C-13 NMR spectra of the sterically hindered chromones were completely assigned using the 2D NOESY, HETCOR, and COLOC spectra. The influence of nonplanar nitro groups on chemical shifts of carbon atoms was studied. Some spectral peculiarities of the peri-methyl group were revealed. The H-1-H-1 and C-13-H-1 spin-spin coupling constants, including the extreme six-bond long-range coupling between the protons of the Me(5) group and H(8), were determined.