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A modified Sandmeyer methodology and the synthesis of (±)-convolutamydine A

✍ Scribed by Simon J. Garden; JoséC. Torres; Alexandre A. Ferreira; Rosangela B. Silva; Angelo C. Pinto


Book ID
104256513
Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
224 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


t:)-Convohtamydine A (5) has been prepared by a concise synthesis from 3,5-dibromoaniline using a modified Sandmeyer methodology. The modified Sandmeyer methodology has also been found to be beneficial for the synthesis of other et-isonitrosoagetanilides. The 4,6-dibromobydroxyoxindole nucleus was further confirmed by comparison with the isomeric 5,7-dibromohydroxyoxindole.


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