Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Milan D. Muškatirović"'
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :1799-1802
The reactivities of 2-substituted cyclohex-1-enylacetic acids with diazodiphenylmethane in eleven alcohols has been investigated. The solvent effect is interpreted in terms of the influence of the relative permittivity on the rate constants. The mult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0e1c34b835ebf26d6d45e37f1042e96
https://doi.org/10.1039/p29940001799
https://doi.org/10.1039/p29940001799
Publikováno v:
ChemInform. 26
The reactivities of 2-substituted cyclohex-1-enylacetic acids with diazodiphenylmethane in eleven alcohols has been investigated. The solvent effect is interpreted in terms of the influence of the relative permittivity on the rate constants. The mult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85cb16dc68fd18cd5ff12dbefbb43b65
https://doi.org/10.1002/chin.199501089
https://doi.org/10.1002/chin.199501089
Autor:
Djordje M. Dimitrijević, Živorad D. Tadić, Milan D. Muškatirović, Mirjana Radojković-Veličković, Milica Mišić-Vuković
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :34-38
The reactivity of a series of substituted pyridine- and N-oxylpyridine-carboxylic acids with diazodiphenylmethane has been investigated and the empirical Hammett treatment applied to a study of substituent effects. In general, satisfactory additivity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b62b133a1effe5fb423f279868ec4f4
https://doi.org/10.1039/p29780000034
https://doi.org/10.1039/p29780000034
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :23-25
In connection with a study of neighbouring double bond participation in cyclopentenylalkyl and cyclohexenylalkyl systems, Taft's σ* constants were determined for cyclopent-1-, -2-, and -3-enyl, cyclopent-1-, -2-, and -3-enylmethyl, cyclohex-1-enyl,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d62c5e9b220e6c631b246b7a92765912
https://doi.org/10.1039/p29790000023
https://doi.org/10.1039/p29790000023
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1257-1259
Two series of NN′-dialkyl derivatives of 2,4-diamino-6-chloro-s-triazines (alkyl groups RCH2CHMe and RCH2CMe2 where R = Me, Et, Pri, or But) were thermally dealkylated, and the mixtures of olefinic products were analysed by g.l.c. In the series of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72ff20f85d545021df8897e351299020
https://doi.org/10.1039/p19770001257
https://doi.org/10.1039/p19770001257
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :1701-1702
A number of primary and secondary NN′-dialkyl derivatives of 2,4-diamino-6-chloro-s-triazines were thermally dealkylated at 250 and 280°. The amount of olefin formed increased in the series of primary derivatives (alkyl = Et, Pr, 2-methylpropyl, 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27b7c2c9f1ade3e159168f48d2f113e5
https://doi.org/10.1039/p29750001701
https://doi.org/10.1039/p29750001701