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1,4-Cycloaddition reactions. II. Preparation of p-dioxino[2,3-g]furo[3,2-c] quinolines, p-dioxino[2,3-f] furo[3,2-c] quinolines, and [1,3] dioxolo[4,5-g] furo[3,2-c] quinolines from 2,3-dihydro-5-methylfuran and schiff bases

✍ Scribed by S. C. Perricone; Edward F. Elslager; Donald F. Worth


Book ID
112122079
Publisher
Journal of Heterocyclic Chemistry
Year
1970
Tongue
English
Weight
362 KB
Volume
7
Category
Article
ISSN
0022-152X

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πŸ“œ SIMILAR VOLUMES


1,4-Cycloaddition reactions. III. Synthe
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## Abstract Synthesis of the linear and angular furoquinolin‐4‐one derivatives 6 and 12 was performed, using nitrobenzofurans 3 and 9 as key intermediates. These compounds were reduced to the corresponding aminobenzofurans 4 and 10, which were condensed in two steps to yield, the linear furoquinoli

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## Abstract The synthesis of [1,4]dioxino[2,3‐__c__]quinolines and [1,4]dioxepino[2,3‐__c__]quinolines with restrained conformation of the piperidine ring, which represent 1,2,3,4‐tetrahydroquinolines containing two heteroatom substituents at positions 3 and 4, is described. In addition, the applic