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Synthesis of ikarugamycin: Model studies on a new strategy for the closure of ring C

✍ Scribed by Raymond C.F. Jones; Richard F. Jones

Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
148 KB
Volume
31
Category
Article
ISSN
0040-4039

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A new modification of the Reissert reaction is reported. On treatment of 2-tosylaminobenzylfurans with ethanolic HCl, some indole derivatives have been obtained. The furan ring served as the origin of a carbonyl group in this reaction.