02255nam 2200541 a 450 991046162270332120200520144314.01-84973-267-1(CKB)2670000000096414(EBL)1185365(OCoLC)723959160(SSID)ssj0000578410(PQKBManifestationID)12225700(PQKBTitleCode)TC0000578410(PQKBWorkID)10577864(PQKB)10706644(MiAaPQ)EBC1185365(PPN)198469721(Au-PeEL)EBL1185365(CaPaEBR)ebr10627623(CaONFJC)MIL872224(EXLCZ)99267000000009641420121208d2011 uy 0engur|n|---|||||txtccrChirality from dynamic kinetic resolution[electronic resource] /Hélène PellissierCambridge [England] RSC Pub.20111 online resource (319 p.)Description based upon print version of record.1-84973-197-7 Includes bibliographical references and index.i-iv; v-vi; vii-x; xi-xiv; xv-xviii; 1-48.pdf; 49-144; 145-190; 191-242; 243-282; 283-284; 285-288; 289-300The last 15 years have witnessed significant developments in the efficiency and scope of the application of DKR. These now offer a serious alternative to conventional methods for asymmetric synthesis. Indeed, impressive examples using new enzymes and major progress in the DKR of racemates have taken place over the past few years. The powerful combination of enzymes and metals has also been the subject of spectacular development. In addition, a new type of DKR, involving organocatalysts, has recently appeared. Although asymmetric catalysis has undergone development during the last two decades, ChiralityElectronic books.Chirality.541.394Pellissier Hélène975910MiAaPQMiAaPQMiAaPQBOOK9910461622703321Chirality from dynamic kinetic resolution2277641UNINA