A one-pot access to cyclopropanes from allylic ethers via hydrozirconation-deoxygenative ring formation.
暂无分享,去创建一个
[1] P. Bertus,et al. Ti(II)-mediated conversion of alpha-heterosubstituted (O, N, S) nitriles to functionalized cyclopropylamines. Effect of chelation on the cyclopropanation step. , 2002, The Journal of organic chemistry.
[2] J. Normant,et al. Use of metallated allylic ethers for the elaboration of vicinally trisubstituted linear substrates or cyclopropyl carbinols , 2000 .
[3] E. Negishi,et al. Alkene and Alkyne Complexes of Zirconocene. Their Preparation, Structure, and Novel Transformations. , 1998 .
[4] A. Dobashi,et al. Hydrozirconation of alkenyloxirane derivatives: Preparation of cycloalkylmethanols , 1998 .
[5] P. Wipf,et al. Kinetic vs. thermodynamic control in hydrozirconation reactions , 1998 .
[6] P. Hodge. Polymer-supported organic reactions: what takes place in the beads? , 1997 .
[7] P. Wipf,et al. SYNTHETIC APPLICATIONS OF ORGANOCHLOROZIRCONOCENE COMPLEXES , 1996 .
[8] E. Negishi,et al. Patterns of Stoichiometric and Catalytic Reactions of Organozirconium and Related Complexes of Synthetic Interest , 1994 .
[9] S. Gronowitz,et al. Hydrozirconation of (E)-3-methoxy-1-phenyl-1-propene and (E)-3-phenyl-2-propenol , 1991 .
[10] C. Krüger,et al. Die reaktivitätsabstufung von trimethylsiloxygruppen gegenüber dem Hydrozirconierungsreagenz Cp2Zr(H)Cl , 1990 .