1975
DOI: 10.1016/0040-4020(75)80002-0
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New synthesis of substituted 3-aryl-1-naphthaldehydes

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1975
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Cited by 10 publications
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“…The 1-naphthalenemethanols prepared for this study are illustrated in Chart I. Synthesis of the 3-aryl-1-naphthalenemethanols (1-6) followed well-known pro-cedures18•9 from the corresponding 3-aryl-1 -naphthaldehydes, syntheses of which have been described. 10 The preparation of the 3-aryloxy (7-11) and 3-aroyl (12) derivatives required a different synthetic sequence, described elsewhere,11 for the preparation of the aldehyde precursers, the 3-bromo-1 -methylnaphthalenes. Conversion of the appropriately substituted 1 -methylnaphthalenes to the naphthaldehydes was accomplished by the steps outlined in Scheme I.…”
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confidence: 99%
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“…The 1-naphthalenemethanols prepared for this study are illustrated in Chart I. Synthesis of the 3-aryl-1-naphthalenemethanols (1-6) followed well-known pro-cedures18•9 from the corresponding 3-aryl-1 -naphthaldehydes, syntheses of which have been described. 10 The preparation of the 3-aryloxy (7-11) and 3-aroyl (12) derivatives required a different synthetic sequence, described elsewhere,11 for the preparation of the aldehyde precursers, the 3-bromo-1 -methylnaphthalenes. Conversion of the appropriately substituted 1 -methylnaphthalenes to the naphthaldehydes was accomplished by the steps outlined in Scheme I.…”
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confidence: 99%
“…Department of Medicinal Chemistry, College of Pharmacy, University of Tennessee Center for the Health Sciences, Memphis, Tennessee 38163. Received April 10,1975 A series of diastereoisomeric 6-benzoyloxy-and 6-benzamido-2-methyldecahydroisoquinolines has been prepared and screened for antiarrhythmic effectiveness. In a continuation of our interest in identifying significant physicochemical properties of antiarrhythmic decahydroisoquinolines, octanol-water partition coefficients and pKa values have been determined for each member of the series.…”
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confidence: 99%