cheminform abstract: the sandmeyer reaction on some selected heterocyclic ring systems: synthesis of...

ChemInform 2010, 41, issue 48 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de General R 0010 DOI: 10.1002/chin.201048085 The Sandmeyer Reaction on Some Selected Heterocyclic Ring Systems: Synthesis of Useful 2-Chloroheterocyclic-3-carbonitrile Intermediates. — The method is successful for various substrate types, although the yields are only moderate to low. In the case of dihydropyridines (XII) and (XIV), aromatization is the only or primary pro- cess. — (DA SILVA, D.; SAMADI*, A.; CHIOUA, M.; CARREIRAS, M. D. C.; MARCO-CONTELLES, J.; Synthesis 2010, 16, 2725-2730, DOI:10.1055/s-0030-1258149 ; Lab. Radicales Libres, Inst. Quim. Org., E-28006 Madrid, Spain; Eng.) — Mais 48- 085

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Page 1: ChemInform Abstract: The Sandmeyer Reaction on Some Selected Heterocyclic Ring Systems: Synthesis of Useful 2-Chloroheterocyclic-3-carbonitrile Intermediates

www.cheminform.wiley-vch.de

GeneralR 0010 DOI: 10.1002/chin.201048085

The Sandmeyer Reaction on Some Selected Heterocyclic Ring Systems: Synthesis of Useful 2-Chloroheterocyclic-3-carbonitrile Intermediates. — The method is successful for various substrate types, although the yields are only moderate to low. In the case of dihydropyridines (XII) and (XIV), aromatization is the only or primary pro-cess. — (DA SILVA, D.; SAMADI*, A.; CHIOUA, M.; CARREIRAS, M. D. C.; MARCO-CONTELLES, J.; Synthesis 2010, 16, 2725-2730, DOI:10.1055/s-0030-1258149 ; Lab. Radicales Libres, Inst. Quim. Org., E-28006 Madrid, Spain; Eng.) — Mais

48- 085

PHOTOREARRANGEMENT OF BICYCLO[2.2.1]HEPTENE-2-CARBONITRILE

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