| Literature DB >> 10649358 |
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Abstract
The new, stable, chiral thiol-TADDOL Cu(I) catalysts 1 (X=OH, OMe, NMe(2)) reveal an unexpected monodentate complexation mode, both in solution and in the solid state. For the first time, the aggregation state of organocopper complexes has been determined by NMR diffusion measurements. NOESY NMR data on model isocyanide Cu complexes reveal a different conformation of the TADDOL moiety as a function of the second potential donor group. TADDOL=alpha,alpha,alpha',alpha'-tetraaryl-2,2-dimethyl-1,3-dioxolane-4,5-dimethanol.Entities:
Year: 2000 PMID: 10649358 DOI: 10.1002/(sici)1521-3773(20000103)39:1<153::aid-anie153>3.0.co;2-n
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336