Alkaline Earth Metal Catalysts for Asymmetric Reactions

Citations Over TimeTop 10% of 2010 papers

Abstract

The group 2 alkaline earth metals calcium (Ca), strontium (Sr), and barium (Ba) are among the most common elements on Earth, abundant in both the sea and the Earth's crust. Although they are familiar in our daily lives, their application to organic synthesis has, so far, been limited. Some particularly useful properties of these elements include (i) low electronegativity, (ii) a stable oxidation state of +2, meaning that they can potentially form two covalent bonds with anions, and (iii) the ability to occupy a variety of coordination sites due to their large ionic radius. Furthermore, the alkaline earth metals, found between the group 1 and group 3 elements, show mild but significant Lewis acidity, which can be harnessed to control coordinative molecules via a Lewis acid-base interaction. Taken together, these characteristics make the metals Ca, Sr, and Ba very promising components of highly functionalized acid-base catalysts. In this Account, we describe the development of chiral alkaline earth metal catalysts for asymmetric carbon-carbon bond-forming reactions. Recently prepared chiral alkaline earth metal complexes have shown high diastereo- and enantioselectivities in fundamental and important chemical transformations. We chose chiral bisoxazoline (Box) derivatives bearing a methylene tether as a ligand for chiral modification. These molecules are very useful because they can covalently coordinate to alkaline earth metals in a bidentate fashion through deprotonation of the tether portion. It was found that chiral calcium-Box complexes could successfully promote catalytic asymmetric 1,4-addition and [3 + 2] cycloaddition reactions with high diastereo- and enantioselectivities. Both the calcium-Box complexes and chiral strontium-bis-sulfonamide and chiral barium-BINOLate complexes could catalyze asymmetric 1,4-addition reactions with high enantioselectivities. Furthermore, we designed a calcium-neutral coordinative ligand complex as a new type of chiral alkaline earth metal catalyst. We found that pyridinebisoxazolines (Pybox) worked well: they served as excellent ligands for calcium compounds in 1,4-addition reactions and Mannich reactions. Moreover, they were successful in 1,4-additions in concert with enantioselective protonation, affording the desired products in good to high enantioselectivities. Our results demonstrate that alkaline earth metals are very useful and attractive catalysts in organic synthesis. Moreover, their ubiquity in the environment is a distinct advantage over rare metals for large-scale processes, and their minimal toxicity is beneficial in both handling and disposal.

Related Papers

• → Convenient synthetic routes to bidentate and monodentate 2-, 3- and 4-pyridyl phosphines: potentially useful ligands for water-soluble complex catalysts(1998)52 cited
• → Superconductivity in Alkaline Earth-Substituted La ₂ CuO _4-y(1987)96 cited
• → Multiple coordination of carbonyl compounds by multidentate main group Lewis acids(1995)50 cited
• → Competitive Coordination of Metals by Phosphorus and Sulfur in Complexes with Polydentate Ligands Containing P(III)-S Bonds(1999)3 cited
• → ChemInform Abstract: Synthesis and Structure of 1,2,3 Superconductors with Alkaline‐Earth Ions.(1990)