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Asymmetric Catalysis

Methodology

The goal of asymmetric catalysis is to synthesize chiral compounds out of achiral substrates. A chiral compound has a unique handedness; it cannot be superimposed upon its mirror image, just as the right hand cannot be superimposed on the left. Many biological molecules are naturally chiral—amino acids and sugars, for instance—and the demand for chiral compounds in the pharmaceutical, agricultural, and chemical industries has been escalating rapidly. Most pharmaceutical drugs, for instance, are now chiral compounds and are usually what are known as single enantiomers, which are composed of only one of the two mirror-image isomers. This month, Special Topics looks at the research trends in asymmetric catalysis over the past decade as well as over the past two years.

In the past decade, the hot research topics in asymmetric catalysis cover a wide spectrum of techniques and catalysts for the synthesis of chiral compounds. Among the many reactions discussed are the asymmetric transition of metal-catalyzed allylic alkylations; the use of chiral ruthernium complexes to affect asymmetric hydrogenation; asymmetric catalysis with water, with optically-active manganese complexes, with proline for catalyzing asymmetric aldol reactions, and with nitrogen-containing ligands, platinum, palladium, and Schiff base catalysts for facilitating asymmetric transfer reactions.

Over the past two years, the list of hot papers in asymmetric catalysis includes those discussing the use of rhodium, praline, and zinc complexes as catalysts. Another area that has generated a handful of hot papers over this period is the direct catalytic asymmetric Mannich-type reactions, which are used for the synthesis of chiral nitrogen-containing compounds. Other research topics on the two-year top 20 list include the use of asymmetric catalysis for the synthesis of aziridines, the synthesis of modified BINOL ligands, and the combination of enzyme and metal catalysts to achieve enantioselective organic reactions.

Methodology

To construct this database, papers were extracted based on title-supplied keywords for Asymmetric Catalysis. The keywords used were as follows: 

asymmetric AND catal*

The baseline time span for this database is 1995-2005 (fourth bimonthly). The resulting database contained 3,668 (10 years) and  1,342 (2 years) papers; 6,297 authors; 52 countries; 189 journals; and 899 institutions.

Rankings

Once the database was in place, it was used to generate the lists of top 20 papers (two- and ten-year periods), authors, journals, institutions, and nations, covering a time span of 1995-2005 (fourth bimonthly, a 10-year + 8-month period).

The top 20 papers are ranked according to total cites. Rankings for author, journal, institution, and country are listed in three ways: according to total cites, total papers, and total cites/paper. The paper thresholds and corresponding percentages used to determine scientist, institution, country, and journal rankings according to total cites/paper, and total papers respectively are as follows:

Entity: Scientists Institutions Countries Journals
Thresholds: 16 19 11 3
Percentage: 1% 5% 50% 50%

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