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Journal ArticleDOI

Asymmetric Catalysis with Heterobimetallic Compounds

Masakatsu Shibasaki, +2 more
- 04 Jul 1997 - 
- Vol. 36, Iss: 12, pp 1236-1256
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TLDR
In this paper, the authors describe the development of rare-earth-alkali metal complexes such as LnM3tris(binaphthoxide) complexes (LnMB, Ln = rare earth metal, M = alkali metal), which are readily prepared from corresponding rare earth trichlorides or rare earth isopropoxides, and their application to catalytic asymmetric synthesis.
Abstract
This review focuses on a new concept in catalytic asymmetric reactions that was first realized for the use of heterobimetallic complexes. As these heterobimetallic complexes function as both a Bronsted base and as a Lewis acid, just like an enzyme, they make possible a variety of efficient catalytic asymmetric reactions. This heterobimetallic concept should prove to be applicable to a variety of new asymmetric catalyses. The first part of this review describes the development of rare-earth–alkali metal complexes such as LnM3tris(binaphthoxide) complexes (LnMB, Ln = rare-earth metal, M = alkali metal), which are readily prepared from the corresponding rare-earth trichlorides or rare-earth isopropoxides, and their application to catalytic asymmetric synthesis. By using a catalytic amount of LnMB complexes several asymmetric reactions proceed efficiently to give the corresponding desired products in up to 98% ee: LnLB-catalyzed asymmetric nitroaldol reactions (L = Li), LnSB-catalyzed asymmetric Michael reactions (S Na), and LnPB-catalyzed asymmetric hydrophosphonylations of either imines or aldehydes (P K). Applications of these heterobimetallic catalysts to the syntheses of several biologically and medicinally important compounds are also described. Spectral analyses and computational simulations of the asymmetric reactions catalyzed by the heterobimetallic complexes reveal that the two different metals play different roles to enhance the reactivity of both reaction partners and to position them. From mechanistic considerations, a useful activation of the heterobimetallic catalyses was realized by addition of alkali metal reagents. The second part describes the development of another type of heterobimetallic catalysts featuring Group 13 elements such as Al and Ga as the central metal. Among them, the AlLibis(binaphthoxide) complex (ALB) is an effective catalyst for asymmetric Michael reactions, tandem Michael–aldol reactions, and hydrophosphonylation of aldehydes.

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Asymmetric catalysis by chiral hydrogen-bond donors.

TL;DR: This review documents the structural and mechanistic features that contribute to high enantioselectivity in hydrogen-bond-mediated catalytic processes in small-molecule, synthetic catalyst systems.
References
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Journal ArticleDOI

UFF, a full periodic table force field for molecular mechanics and molecular dynamics simulations

TL;DR: In this article, the Universal force field (UFF) is described, where the force field parameters are estimated using general rules based only on the element, its hybridization, and its connectivity.
Journal ArticleDOI

Biological activity of aminophosphonic acids

TL;DR: Aminophosphonates are analogues of amino acids in which a carboxylic moiety is replaced by phosphonic acid or related groups that inhibit enzymes involved in amino acid metabolism and thus affect the physiological activity of the cell.
Journal ArticleDOI

Application of a universal force field to organic molecules

TL;DR: In this paper, the Universal Force Field (UFF) was used to predict the structures of a variety of organic molecules, including unstrained and uncongested hydrocarbons, silanes, alkenes, saturated amines, saturated ethers and phosphines.
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