1982
DOI: 10.1080/00397918208080061
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A Malonic Ester Synthesis with Acid Chlorides. The Homologation of Oioic Acids

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Cited by 21 publications
(2 citation statements)
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“…In another approach to 6, we planned the acylation of key intermediate (3); which would demonstrate the utility of Meldrum's acid (1) in the synthesis of desired ketones. The reaction in fact, represents the stepwise monoalkylation 27 and acylation [34][35][36] of Meldrum's acid. The key intermediate 3 was condensed with 3,3-dimethylacryloyl chloride in dichloromethane and pyridine to give the alkyl acyl Meldrum's acid 7.…”
mentioning
confidence: 99%
“…In another approach to 6, we planned the acylation of key intermediate (3); which would demonstrate the utility of Meldrum's acid (1) in the synthesis of desired ketones. The reaction in fact, represents the stepwise monoalkylation 27 and acylation [34][35][36] of Meldrum's acid. The key intermediate 3 was condensed with 3,3-dimethylacryloyl chloride in dichloromethane and pyridine to give the alkyl acyl Meldrum's acid 7.…”
mentioning
confidence: 99%
“…modified this procedure, replacing the difficultly available malonyl dibromide by a mixture of malonyl dichloride and gaseous HBr. The subsequent reaction of 3 with Meldrum's ester, 4, 10 yielded the diketone 1 in a low yield (~10 %). A low yield (also under 10%) also was obtained when the lithium salt of acetylacetic acid was reacted with azulene in the presence of oxalyl chloride (Scheme 1).…”
Section: Introductionmentioning
confidence: 99%