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A flexible, convergent route to azaoxindoles, azaindolines, azaindoles, and tetrahydroazaquinolones

E. Bacqué 1 Myriem El Qacémi 2, 3 Samir Zard 3
1 Sanofi-Aventis [Toulouse]
2 Syngenta Crop Protection AG
3 DCSO - Laboratoire de synthèse organique
Abstract : A variety of azaoxindoles, azaindolines, azaindoles, and tetrahydroazaquinolones can be readily prepared by cyclisation onto pyridine rings of radicals derived from xanthates. The xanthate precursors may themselves be produced by intermolecular radical addition-transfer to allylamino- or butenoylamide side-chains. © 2012 The Japan Institute of Heterocyclic Chemistry.
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Submitted on : Tuesday, February 25, 2014 - 9:52:08 PM
Last modification on : Thursday, March 5, 2020 - 6:25:14 PM

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CNRS | X-DCSO | X | INC-CNRS | X-DEP-CHIM

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E. Bacqué, Myriem El Qacémi, Samir Zard. A flexible, convergent route to azaoxindoles, azaindolines, azaindoles, and tetrahydroazaquinolones. Heterocycles, The Japan Institute of Heterocyclic Chemistry, 2011, 84 (1), pp.291-299. ⟨10.3987/com-11-s(p)24⟩. ⟨hal-00950005⟩

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