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- W2242809612 endingPage "198" @default.
- W2242809612 startingPage "115" @default.
- W2242809612 abstract "Chirality plays a central role in chemical science and related technologies. Until the early 1970s, access to highly enantiomerically pure compounds from prochiral precursors, at least in a practical sense, was considered viable only by biological or enzymatic methods. However, recent dramatic progress in stereoselective organic synthesis is converting the chemists’ dream into reality. Particularly, homogeneous asymmetric catalysis using chiral metal complexes is an ideal way in this context, and provides powerful tools complementary to biological transformations, structural modification of naturally occurring chiral substances, and classical resolution methods. In principle, rational molecular architecture can create any chemical functions at will and the catalysis, unlike ordinary stoichiometric asymmetric synthesis, is capable of multiplying chirality. The efficiency of the chiral multiplication, defined as [major enantiomer — minor enantiomer (in mole)]/chiral source in mole, can be infinite. Here the selection of central metals and molecular designing of the chiral modifiers are particularly significant. The ligands or auxiliaries modifying intrinsically achiral metal atoms must be endowed with suitable functionality, configuration, and conformational rigidity or flexibility, depending on the cases, all of which contribute to accomplish desirable stereoselection.1)" @default.
- W2242809612 created "2016-06-24" @default.
- W2242809612 creator A5010969676 @default.
- W2242809612 creator A5054350731 @default.
- W2242809612 date "1989-01-01" @default.
- W2242809612 modified "2023-10-06" @default.
- W2242809612 title "Enantioselective Catalysis with Metal Complexes. An Overview" @default.
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