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Synlett 2004(11): 1905-1908
DOI: 10.1055/s-2004-830868
DOI: 10.1055/s-2004-830868
LETTER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Indoles Using Cyclization of Imidoyl Radicals
Weitere Informationen
Received
20 May 2004
Publikationsdatum:
04. August 2004 (online)
Publikationsverlauf
Publikationsdatum:
04. August 2004 (online)

Abstract
Imidoyl radicals, generated from imidoyl phenylselanide precursors, have been used for the synthesis of 2,3-disubstituted indoles. A facile high yielding synthesis of imidoyl phenylselanides has been developed. The potential for neophyl rearrangement of 5-exo radical intermediates to 6-endo radical intermediates is discussed.
Key words
radicals - radical reactions - indoles - cyclizations - rearrangements
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References
We thank Professor Mario D. Bachi, Weizmann Institute, Rehevot, Israel for providing us with unpublished results.