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Synthesis 1998; 1998(4): 393-404
DOI: 10.1055/s-1998-2044
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1,3-Dipolar Cycloaddition Reaction of 3,4-Dihydro-β-carboline 2-Oxide

Satoshi Moriyama* , Yannick Vallée
  • *L.E.D.S.S., UMR Université Joseph Fourier-CNRS, B.P. 53, F-38041 Grenoble, France; Fax + 33(4)76 51 43 82; E-mail: yannick.vallee@ujf-grenoble.fr
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Publication History

Publication Date:
31 December 2000 (online)

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3,4-Dihydro-β-carboline 2-oxide (1) undergoes 1,3-dipolar [3+2] cycloaddition reactions with a variety of dipolarophiles to give the corresponding cycloadducts 2-26′. The regio- and stereoselectivities concerning these cycloaddition reactions are studied.

1,3-dipolar cycloadditions - nitrones - regioselectivity - stereoselectivity - 9H-pyrido[3,4-b]indoles

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