4481-35-0Relevant articles and documents
Eine verbesserte Synthese des 2-Oxocycloheptafurans
Wetzel, Arthur,Lewars, Errol G.,Zeller, Klaus-Peter
, p. 945 - 946 (1983)
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An efficient preparation of 2H-cyclohepta[b]furan-2-ones
Morita, Noboru,Kudo, Masao,Yokoyama, Ryuji,Ito, Shunji
, p. 679 - 689 (2007/10/03)
2H-cyclohepta[b]furan-2-one (3) was prepared in high yield from a [2+2] cycloadduct between cycloheptatriene and dichloroketene by Baeyer-Villiger oxidation followed by dehydrochlorination. 3-Chloro- (8) and 6-chloro-2H-cyclohepta[b]furan-2-one (9) were obtained from the [2+2] cycloadduct by adding an epoxidation step to the above synthetic way in moderate yields.
Reaction of 2,2,2-Triphenyl-2H-6,11-methanocycloundec-1,2λ5-oxaphosphole (2-Triphenylphosphoranylidenemethyl-5,10-methanoannulenone) and Its Related Compounds with Heterocumulenes
Nitta, Makoto,Naya, Shin-ichi
, p. 2363 - 2380 (2007/10/03)
Reactions of 2,2,2-triphenyl-2H-6,11-methanocycloundec-1,2λ5-oxaphosphole annulenone> 8 and 2-(triphenyl-phosphoranylidenemethyl)tropones 9a-c with heterocumulenes have been studied to provide evidence for a P---O bonding betaine and to explore a preparative method for annulated heterocycles. The reaction of 8 with phenyl isocyanate 2 afforded N-phenyl-2H-6,11-methanocycloundecapyrrol-2-one in good yield, while that with phenyl isothiocyanate 4 afforded N-phenyl-2H-6,11-methanocycloundecapyrrol-2-thione and 2-(N-phenylamino)-4H-6,11-methanocycloundecathiophen-4-one in good combined yield. On the other hand, the reaction of 2-triphenylphosphoranylidenemethyltropone 9a, its ethoxycarbonyl- and cyano-substituted derivatives 9b,c with the isocyanate 2 gave 2H-cycloheptafuran-2-ones along with N-phenyl-2H-cycloheptafuran-2-imines, which are obtained by the reaction of compounds 9a,b with diphenylcarbodiimide 3. On the other hand, the reaction of compound 9a with the isothiocyanate 4 afforded 2-(N-phenylamino)-4H-cycloheptathiophen-4-one in addition to N-phenyl-2H-cycloheptafuran-2-imine, while compounds 9b,c reacted with the isothiocyanate 4 to give 2H-cycloheptafuran-2-thiones along with N-phenyl-2H-cycloheptafuran-2-imines. The reaction pathways and the important behavior of a P---O bonding structure for 8, as compared to that for 9a-c, are discussed on the basis of the 31P NMR spectral data and product analyses.
Synthesis and analysis of positive inotropic effects of 3-substituted-2H-cyclohepta[b]furan-2-one derivatives
Yokota,Yanagisawa,Kosakai,Wakabayashi,Tomiyama,Yasunami
, p. 865 - 871 (2007/10/02)
Several 3-substituted-2H-cyclohepta[h]furan-2-one derivatives were prepared and tested in vitro for positive inotropic character. Introduction of an isopropyl group at the 5-position of compound 8a caused an increase of PIC50 (negative logarithm of the dosage which increases the contractile force by 50%) from 4.48 to 5.10. Among the 5-isopropyl-8-alkoxy compounds, the isopropoxy compound 12f had the most potent activity with a PIC50 value of 5.99. Conversion of the ester group at the 3-position to a methylene group and of the alkoxy group at the 8-position to a substituted amino group caused a decrease in activity. The most active compound, 12f, was also found to bave a weaker heart rate (HR)-increasing effect compared to milrinone and amrinone.