Literature DB >> 15917900

Catalytic asymmetric cyclopropanation at a chiral platform.

Jian Gao1, F Ross Woolley, Ralph A Zingaro.   

Abstract

Novel chiral Robson-type macrocyclic complexes M(2)-L [where M = Mn(II), Mn(III), Co(II) and Co(III) and L denotes tetra-Schiff base chiral ligands, L1 or L2] have been synthesized by metal template condensation of 2,6-diformyl-4-methyl-phenol, with 1R,2R-diaminocyclohexane (L1) or 1R,2R-diphenylethylenediamine (L2). The dinuclear Co(II) and Co(III) complexes catalyze asymmetric cyclopropanation of styrene with diazoacetate cooperatively and with high enantioselectivity.

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Year:  2005        PMID: 15917900     DOI: 10.1039/b503971a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Catalytic asymmetric 1,4-additions of beta-keto esters to nitroalkenes promoted by a bifunctional homobimetallic Co2-Schiff base complex.

Authors:  Makoto Furutachi; Zhihua Chen; Shigeki Matsunaga; Masakatsu Shibasaki
Journal:  Molecules       Date:  2010-01-22       Impact factor: 4.411

Review 2.  Imine- and Amine-Type Macrocycles Derived from Chiral Diamines and Aromatic Dialdehydes.

Authors:  Jerzy Lisowski
Journal:  Molecules       Date:  2022-06-25       Impact factor: 4.927

  2 in total

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