Facile Synthesis of Some Novel Dicarboxylic Acid Crown Ethers
نویسندگان
چکیده
منابع مشابه
Crown Ethers in Enantioselective Synthesis
A number of new chiral crown compounds and lariat ethers have been synthesized starting from phenyl-D-glucopyranoside, methyl-D-glucopyranoside and galactopyranoside, methyl-D-mannopyranoside and 1,2:5,6-di-O-isopropylidene-D-mannitol, but the main emphasis was laid on their application. Some of the sugar-based macrocycles showed significant asymmetric induction as phase transfer catalysts in l...
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The ability of macroheterocyclic compounds to complex with ionic species has led to the synthesis and investigation of many multidentate macroheterocyclic species . The most stable complexes are formed between macrocyclic polyetheral ligands (crown ethers) with alkali or alkaline earth metal iona. There is an excellent correlation of the stability of these complexes with the size of the cation ...
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Two series of novel derivatives of pyridine-2,6-dicarboxylic acid with potential as polydentate ligands were synthesized from pyridine-2,6-dicarboxylic acid. All new compounds were characterized by NMR, MS, IR, and EA.
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The methodology involves preparing polyvinyl sulfuric acid as a solid acid by simple mixing ofpolyvinyl alcohol with chlorosulfonic acid in CH2Cl2 at room temperature. The catalytic ability ofthe solid acid was investigated for the facile conversion of benzylic alcohols to the unsymmetricalethers with aliphatic alcohols in the presence of the solid acid. Results show that the solid acid isan ap...
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A benign and efficient synthesis of chiral macrocyclic 'aza-crown' ethers of varying ring size is reported. The synthesis involves a Schiff base condensation of ether linked dialdehydes of varying chain length and (1R,2R)-(-)-1,2-diaminocyclohexane under mild conditions to yield the macrocycles, which are subsequently reduced to yield the diamino analogues.
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ژورنال
عنوان ژورنال: Journal of Chemical Research
سال: 1999
ISSN: 1747-5198,2047-6507
DOI: 10.1177/174751989902300135