Enzyme-Catalyzed Irreversible Acyl Transfer

(opens in new window) Buy Article (opens in new window) Permissions and Reprints (opens in new window) All articles of this category (opens in new window) This paper reviews the present state of enzyme-catalyzed acyltransfer reactions, which represent a highly useful method for the transformation of alcoholic and amino functional groups in a chemo-, regio- and enantioselective fashion. 1. Introduction 2. Acyl-Transfer Techniques 2.1. Quasi-Irreversible Acyl Donors 2.2. Irreversible Acyl Donors 2.3. Other Acyl Donors 3. Synthetic Applications 3.1. Separation of E / Z -Stereoisomers 3.2. Asymmetrization of Prochiral or meso -Diols 3.3. Enzymatic Resolution of Primary and Secondary Alcohols 3.4. Enzymatic Resolution of Labile Hydroxy Compounds 3.5. Regioselective Protection of Polyhydroxy Compounds 3.5.1. Enzymatic Acylation of Carbohydrates 3.5.2. Enzymatic Acylation of Natural Glycosides 3.5.3. Regio- and Chemoselective Acylation of Alkaloids 3.5.4. Regioselective Acylation of Polyhydroxy Steroids 4. Preparative Procedures 5. Final Remarks