A New General Route to Thiophenophanes: Synthesis and Properties of [n](2,5)Thiophenophane-1,n-diones
摘要:
A series of [ n]( 2,5) thiophenophane-1, n-diones ( 5) ( n = 9, 10, 12, 14, 16, and 20) were synthesized in a simple four-step route starting from the appropriate 1,omega-oligomethylenedicarboxylic acids. The bis-( halomethylketones) ( 6), which were obtained by successive treatment of the diacids with SOCl2, diazomethane, and HBr or HCl, were cyclized by Na2S under high dilution conditions. The obtained monomeric cyclic diketosulfides ( 4) were condensed with glyoxal in MeOH by slowly adding dilute NaOMe affording 5. The thiophene-2,5-dicarbonyl moiety of 5 ( n = 9) is significantly deformed as shown by X-ray crystallography, and the effect of the strain is reflected in the C=O stretching frequencies and the pi-pi* and the n-pi* absorptions.
A New General Route to Thiophenophanes: Synthesis and Properties of [n](2,5)Thiophenophane-1,n-diones
摘要:
A series of [ n]( 2,5) thiophenophane-1, n-diones ( 5) ( n = 9, 10, 12, 14, 16, and 20) were synthesized in a simple four-step route starting from the appropriate 1,omega-oligomethylenedicarboxylic acids. The bis-( halomethylketones) ( 6), which were obtained by successive treatment of the diacids with SOCl2, diazomethane, and HBr or HCl, were cyclized by Na2S under high dilution conditions. The obtained monomeric cyclic diketosulfides ( 4) were condensed with glyoxal in MeOH by slowly adding dilute NaOMe affording 5. The thiophene-2,5-dicarbonyl moiety of 5 ( n = 9) is significantly deformed as shown by X-ray crystallography, and the effect of the strain is reflected in the C=O stretching frequencies and the pi-pi* and the n-pi* absorptions.
The Acid Catalyzed Decomposition of Diazo Compounds. I. Synthesis of Oxazoles in the BF<sub>3</sub>Catalyzed Reaction of Diazo Carbonyl Compounds with Nitriles
作者:Toshikazu Ibata、Ryohei Sato
DOI:10.1246/bcsj.52.3597
日期:1979.12
The BF3-catalyzed decomposition of diazo carbonyl compounds in nitriles have afforded the corresponding oxazoles in high yields. This method is applicable to diazo carbonyl compounds such as m- and p-substituted diazoacetophenones, ethyl diazoacetate, 1,2-diphenyl-2-diazoethanone, dibenzoyldiazomethane, and dimethyl diazomalonate. Bis(diazo ketone)s such as terminal bis(diazoacetylated) alkanes (III1−4:
Synthesis of some medium- and large-ring cycloalk-2-ene-1,4-diones by intramolecular coupling of αω-bis-diazoketones
作者:Sunanta Kulkowit、M. Anthony McKervey
DOI:10.1039/c39780001069
日期:——
In the presence of Cu(acac)2(Hacac = acetylacetone) someαω-bis-diazoketones couple intramolecularly with loss of nitrogen giving cycloalk-2-ene-1,4-diones; the enediones can be converted into fused ring cyclopentenones by successive treatment with sodium dithionite and sodium hydroxide.