On the Synthesis of cis-Dicarboxylic Acid Anhydrides
نویسندگان
چکیده
منابع مشابه
Stereospecific synthesis of azetidine-cis-2,3-dicarboxylic acid.
Electrocyclic reaction product of 1-(methoxycarbonyl)-1,2-dihydropyridine was stereospecifically converted by RuO(4) oxidation into azetidine-cis-2,3-dicarboxylic acid.
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In the title compound, C(8)H(12)O(4), the two carboxyl groups are on the same side of the cyclohexane ring and the ring adopts a chair conformation. Adjacent mol-ecules related by an inversion centre are linked by pairs of O-H⋯O hydrogen bonds, forming a zigzag chain along [1].
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چکیده ندارد.
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ژورنال
عنوان ژورنال: NIPPON KAGAKU KAISHI
سال: 1937
ISSN: 0369-4208,2185-0909
DOI: 10.1246/nikkashi1921.58.10_1089