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51.
Frank A. L. Anet N. Roy Easton Issa Yavari 《Magnetic resonance in chemistry : MRC》1979,12(5):299-301
The natural-abundance 13C NMR spectra of cis,cis-1,5-cyclooctadiene monoepoxide and cis,syn,cis-1,5-cyclooctadiene diepoxide have been investigated over the temperature range of – 10 to – 180°C. Whereas the spectra of the former showed no dynamic NMR effect, two different conformations in the ratio of 3:1 were observed at low temperatures for the latter. The free-energy barrier (ΔG≠) for conversion of the major conformation to the minor conformation is calculated to be 5.9°0.2 kcal mol?1 from a line-shape analysis of spectra obtained at intermediate temperatures. It is shown that cis,syn,cis-1,5-cyclooctadiene diepoxide exists in solution in chair (major) and in twist-boat (minor) conformations of slightly different energies. Interconversion paths between these conformations are discussed. The monoepoxide is suggested to have a twist-boat conformation that is rapidly pseudorotating via a boat conformation even at – 180°C. 相似文献
52.
The 13C n.m.r. spectrum of benzofuroxan at ?15°C is assigned on the basis of selective decoupling experiments and by comparison with the 13C chemical shifts of model compounds. The 13C spectra were also measured in trifluoroacetic acid as a solvent. From the temperature dependence of the 13C spectrum of benzofuroxan in CDCl3, a barrier of 14·0 ± 0·2 kcal mol?1 is obtained for the degenerate tautomerism in this compound. 相似文献
53.
Issa?YavariEmail author Hoorieh?Djahaniani Farough?Nasiri 《Monatshefte für Chemie / Chemical Monthly》2004,135(5):543-548
Summary. The 1:1 reactive intermediate generated by the addition of alkyl isocyanides to dialkyl acetylenedicarboxylates was trapped by fairly strong NH-acids such as carbazole, indole, or pyrrole to yield highly functionalized 1-azadienes and ketenimines. 相似文献
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56.
Issa Yavari Mohammad Anary-Abbasinejad Abdolali Alizadeh 《Monatshefte für Chemie / Chemical Monthly》2002,15(1):1331-1336
Protonation of the reactive intermediate produced in the reaction between pyridine and dialkyl acetylenedicarboxylates by strong CH-acids such as N,N′-dimethylbarbituric acid, Meldrum’s acid, or indane-1,3-dione leads to a vinylpyridinium cation which undergoes an addition reaction with the enolate anion of the CH-acid to produce stable 1,4-diionic pyridinium betaines in good yields. 相似文献
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Issa Yavari Maryam Sabbaghan Zinatossadat Hossaini Majid Ghazanfarpour‐Darjani 《Helvetica chimica acta》2008,91(6):1144-1147
Triphenyl phosphite reacts smoothly with dialkyl acetylenedicarboxylates and hexachloroacetone to produce alkyl 2‐(dichloromethylene)‐2,5‐dihydro‐5‐oxo‐4‐(trichloromethyl)furan‐3‐carboxylates in good yields. 相似文献
59.
Efficient reaction conditions have been developed to prepare highly functionalized chiral pyranosido-pyrimidine by regioselective alkylation of the pyranoside ring and palladium-catalyzed cross-coupling reaction on the pyrimidine ring under microwave activation. Such scaffold contains three different functions suitable for selective derivatization and could find applications in the design of peptidomimetics. 相似文献
60.
Issa Yavari Ako Mokhtarporyani-Sanandaj Loghman Moradi Anvar Mirzaei 《Tetrahedron》2008,64(22):5221-5225
The 1:1 intermediate generated by the addition of alkyl(aryl) isocyanides to dimethyl acetylenedicarboxylate is trapped by benzoyl chloride to yield functionalized 2,5-dihydro-1H-pyrroles. The presence of electron-withdrawing groups at the para position of benzoyl chloride leads to tetrasubstituted furans. The structures of these products were confirmed by single-crystal X-ray diffraction studies. 相似文献