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035   $a(OCoLC)723959160
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035   $a(PQKBTitleCode)TC0000578410
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100   $a20121208d2011      uy             0
101 0 $aeng
135   $aur|n|---|||||
181   $ctxt
182   $cc
183   $acr
200 10$aChirality from dynamic kinetic resolution$b[electronic resource] /$fHe?le?ne Pellissier
210   $aCambridge [England] $cRSC Pub.$d2011
215   $a1 online resource (319 p.)
300   $aDescription based upon print version of record.
311   $a1-84973-197-7 
320   $aIncludes bibliographical references and index.
327   $ai-iv; v-vi; vii-x; xi-xiv; xv-xviii; 1-48.pdf; 49-144; 145-190; 191-242; 243-282; 283-284; 285-288; 289-300
330   $aThe 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, 
606   $aChirality
608   $aElectronic books.
615  0$aChirality.
676   $a541.394
700   $aPellissier$b He?le?ne$0975910
801  0$bMiAaPQ
801  1$bMiAaPQ
801  2$bMiAaPQ
906   $aBOOK
912   $a9910461622703321
996   $aChirality from dynamic kinetic resolution$92277641
997   $aUNINA