Interaction of fluorine-containing 1,3-dicarbonyl compounds with polyamines
摘要:
In the reaction of fluorinated copper(II) 1,3-diketonates with diethylenetriamine (or triethylenetetramine) in CHCl3, N,N'-bis(1,3-aminovinylketones) are formed in 21-35% yields. Fluorine-containing 1,3-diketones and 1,3-ketoesters, upon interaction with polyamines without solvent, undergo acid cleavage, forming the corresponding amides. The copper(II) 1,3-ketoesterates are readily cleaved in CHCl3 at 25-degrees-C in excess triethylenetetramine or ethylenediamine.
Condensation of fluoroalkyl-containing 1,3-dicarbonyl compounds with ethylenediamine
作者:V.I. Saloutin、Z.E. Skryabina、Y.V. Burgart
DOI:10.1016/s0022-1139(00)81181-1
日期:1992.3
interaction of fluoroalkylated 1,3-diketones with ethylenediamine hydroperchlorate; similarly, 1,2,3,4-tetrahydro-1,4-diazepine-5-ones have been obtained from fluorinated 1,3-keto esters. Under mild conditions, fluorinated copper(II) 1,3-diketonates, and copper(II) and nickel(II) N,N′-ethylenebis(aminovinyl ketonates) were found to react with ethylenediamine to form fluoroalkyl-containing N,N′-ethylenebis(aminovinyl
通过氟烷基化的1,3-二酮与乙二胺氢氯酸盐的直接相互作用制备了2,3-二氢-1 H -1,4-二氮杂pine;类似地,已经从氟化的1,3-酮酯获得了1,2,3,4-四氢-1,4-二氮杂-5-酮。在温和的条件下,发现氟化的1,3-二酮铜(II)和N(N)的铜(II)和N'-亚乙基双(氨基乙烯基酮)会与乙二胺反应生成含氟烷基的N,N' -亚乙基双(氨基乙烯基酮)和/或2,3-二氢-1 H -1,4-二氮杂s 。
2-Acetyl-substituted polyfluorinated ?-keto esters in reaction with amines
作者:K. I. Pashkevich、V. M. Krokhalev、V. I. Saloutin
DOI:10.1007/bf00961931
日期:1988.6
PASHKEVICH, K. I.;KROXALEV, V. M.;SALOUTIN, V. I., IZV. AN CCCP. CEP. XIM.,(1988) N 6, 1367-1371
作者:PASHKEVICH, K. I.、KROXALEV, V. M.、SALOUTIN, V. I.
DOI:——
日期:——
Interaction of fluorine-containing 1,3-dicarbonyl compounds with polyamines
作者:V. I. Saloutin、Z. �. Skryabina、Ya. V. Burgart、S. V. Kiseleva
DOI:10.1007/bf00863371
日期:1992.11
In the reaction of fluorinated copper(II) 1,3-diketonates with diethylenetriamine (or triethylenetetramine) in CHCl3, N,N'-bis(1,3-aminovinylketones) are formed in 21-35% yields. Fluorine-containing 1,3-diketones and 1,3-ketoesters, upon interaction with polyamines without solvent, undergo acid cleavage, forming the corresponding amides. The copper(II) 1,3-ketoesterates are readily cleaved in CHCl3 at 25-degrees-C in excess triethylenetetramine or ethylenediamine.