Your browser doesn't support javascript.
loading
Asymmetric Intramolecular Buchner Reaction: From High Stereoselectivity to Coexistence of Norcaradiene, Cycloheptatriene, and an Intermediate Form in the Solid State.
Darses, Benjamin; Maldivi, Pascale; Philouze, Christian; Dauban, Philippe; Poisson, Jean-François.
Afiliação
  • Darses B; Univ. Grenoble Alpes, CNRS, DCM, 38000 Grenoble, France.
  • Maldivi P; Institut de Chimie des Substances Naturelles, CNRS UPR-2301, Université Paris-Sud, Université Paris-Saclay, 1 av. de la Terrasse, 91198 Gif-sur-Yvette, France.
  • Philouze C; Univ. Grenoble Alpes, CEA, CNRS, IRIG, SyMMES, 38000 Grenoble, France.
  • Dauban P; Univ. Grenoble Alpes, CNRS, DCM, 38000 Grenoble, France.
  • Poisson JF; Institut de Chimie des Substances Naturelles, CNRS UPR-2301, Université Paris-Sud, Université Paris-Saclay, 1 av. de la Terrasse, 91198 Gif-sur-Yvette, France.
Org Lett ; 23(2): 300-304, 2021 Jan 15.
Article em En | MEDLINE | ID: mdl-33393310
Bicyclic compounds bearing a quaternary stereogenic center have been obtained using asymmetric intramolecular Buchner reaction with excellent yields and level of enantioselectivity. X-ray crystallography determination of the absolute configuration of one product has led to the serendipitous observation of an unusual behavior within the crystal structure, with equilibrating norcaradiene and cycloheptatriene valence isomers at the solid state, as well as an even more unexpected intermediate form. DFT calculations were performed to support these observations.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article