N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide

نویسنده

  • Jian Li
چکیده

In the title racemic compound, C(14)H(10)ClNO(3), which contains four stereogenic centres, the cyclo-hexane ring tends towards a boat conformation, while the tetra-hydro-furan and dihydro-furan rings adopt envelope conformations. The dihedral angle between the mean planes of the pyrrolidine-2,5-dione unit and the 4-chloro-phenyl ring is 49.0 (2)°.

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منابع مشابه

N-Carbamothioyl­amino-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide

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Biological activity of novel N-substituted amides of endo-3-(3-methylthio-1,2,4-triazol-5-yl)bicyclo[2.2.1]hept-5-ene-2-carboxylic acid and N-substituted amides of 1-(5-methylthio-1,2,4-triazol-3-yl)cyclohexane-2-carboxylic acids.

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Benzothia­zol-2-amine–3-meth­oxy­carbonyl-7-oxabicyclo­[2.2.1]hept-5-ene-2-carb­oxy­lic acid (1/1)

In the title 1:1 adduct, C(7)H(6)N(2)S·C(9)H(10)O(5), all non-H atoms of the benzothia-zol-2-amine mol-ecule are essentially coplanar, with a maximum deviation of 0.0286 (9) Å for the S atom. In the crystal, inter-molecular N-H⋯O and O-H⋯N hydrogen bonds connect two mol-ecules of each type into centrosymmetric four-component clusters.

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An unexpected formation of the novel 7-oxa-2-azabicyclo[2.2.1]hept-5-ene skeleton during the reaction of furfurylamine with maleimides and their bioprospection using a zebrafish embryo model.

An unexpected intramolecular cyclization during the reaction of furfurylamine with maleimides is reported as a novel strategy for the efficient green synthesis of the 7-oxa-2-azabicyclo[2.2.1]hept-5-ene skeleton. Under the same reaction conditions, 7-oxabicyclo[2.2.1]hept-5-enes were synthesized when furfurylamine was N-protected by the acetyl group. Both types of bicycloheptenes were screened ...

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عنوان ژورنال:

دوره 66  شماره 

صفحات  -

تاریخ انتشار 2010