LEADER 05844nam 22008413u 450 001 996218171503316 005 20230617011948.0 010 $a1-280-27032-2 010 $a9786610270323 010 $a0-470-36296-0 010 $a0-470-85579-7 010 $a0-470-85580-0 035 $a(CKB)111087027148366 035 $a(EBL)153812 035 $a(OCoLC)807996068 035 $a(SSID)ssj0000291044 035 $a(PQKBManifestationID)11217254 035 $a(PQKBTitleCode)TC0000291044 035 $a(PQKBWorkID)10249037 035 $a(PQKB)10569495 035 $a(MiAaPQ)EBC153812 035 $a(EXLCZ)99111087027148366 100 $a20131014d2003|||| u|| | 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCatalysts for fine chemical synthesis$b[electronic resource] $ehydrolysis, oxidation and reduction 210 $aHoboken $cWiley$d2003 215 $a1 online resource (245 p.) 225 1 $aCatalysts For Fine Chemicals Synthesis ;$vv.7 300 $aDescription based upon print version of record. 311 $a0-471-98123-0 327 $aCatalysts for Fine Chemical Synthesis Volume 1; Contents; Series Preface; Preface to Volume 1; Abbreviations; PART I: REVIEW; 1 The Integration of Biotransformations into the Catalyst Portfolio; 1.1 Hydrolysis of esters, amides, nitriles and oxiranes; 1.2 Reduction reactions; 1.2.1 Reduction of carbonyl compounds; 1.2.2 Reduction of alkenes; 1.3 Oxidative transformations; 1.4 Carbon-carbon bond-forming reactions; 1.5 Conclusions; References; PART II: PROCEDURES; 2 General Information; 3 Asymmetric Epoxidation; 3.1 Introduction; References; 4 Epoxidation of a, b-Unsaturated Carbonyl Compounds 327 $a4.1 Non-asymmetric epoxidation4.2 Asymmetric epoxidation using poly-D-leucine; 4.2.1 Synthesis of leucine N-carboxyanhydride; 4.2.2 Synthesis of immobilized poly-D-leucine; 4.2.3 Asymmetric epoxidation of (E)-benzylideneacetophenone; 4.2.4 Conclusion; 4.3 Asymmetric epoxidation using chiral modified diethylzinc; 4.3.1 Epoxidation of 2-isobutylidene-1-tetralone; 4.3.2 Conclusion; 4.4 Asymmetric epoxidation of (E)-benzylideneacetophenone using the La-(R)-BINOL-Ph(3)PO/cumene hydroperoxide system; 4.4.1 Merits of the system; References; 5 Epoxidation of Allylic Alcohols 327 $a5.1 Non-asymmetric epoxidation5.2 Asymmetric epoxidation using a chiral titanium complex; 5.2.1 Epoxidation of cinnamyl alcohol; 5.2.2 Epoxidation of (E)-2-methyl-3-phenyl-2-propenol; 5.2.3 Epoxidation of (E)-2-hexen-1-ol; 5.2.4 Conclusion; 5.3 Asymmetric epoxidation of (E)-undec-2-en-1-ol using poly(octamethylene tartrate); 5.3.1 Synthesis of branched poly (octamethylene-L-(+)-tartrate); 5.3.2 Asymmetric epoxidation of (E)-undec-2-en-1-ol; References; 6 Epoxidation of Unfunctionalized Alkenes and a, b-Unsaturated Esters 327 $a6.1 Asymmetric epoxidation of disubstituted Z-alkenes using a chiral salen-manganese complex6.1.1 Epoxidation of (Z)-methyl styrene; 6.1.2 Epoxidation of (Z)-ethyl cinnamate; 6.1.3 Conclusion; 6.2 Asymmetric epoxidation of disubstituted E-alkanes using a D-fructose based catalyst; 6.2.1 Epoxidation of (E)-stilbene; 6.2.2 Conclusion; 6.3 Enantioselective epoxidation of (E)-b-methylstyrene by D(2)-symmetric chiral trans-dioxoruthenium (VI) porphyrins; 6.3.1 Preparation of the trans-dioxoruthenium(VI) complexes with D(2)-symmetric porphyrins (H(2)L(1-3)) 327 $a6.3.2 Enantioselective epoxidation of (E)-b-methylstyrene6.3.3 Conclusion; References; 7 Asymmetric Hydroxylation and Aminohydroxylation; 7.1 Asymmetric aminohydroxylation of 4-methoxystyrene; 7.1.1 Conclusion; 7.2 Asymmetric dihydroxylation of (1-cyclohexenyl)acetonitrile; 7.2.1 (R,R)-(1,2-Dihydroxycyclohexyl)acetonitrile acetonide; 7.2.2 Conclusion; References; 8 Asymmetric Sulfoxidation; 8.1 Asymmetric oxidation of sulfides and kinetic resolution of sulfoxides; 8.1.1 Asymmetric oxidation of 4-bromothioanisole; 8.1.2 Kinetic resolution of racemic 4-bromophenyl methyl sulfoxide; References 327 $a9 Asymmetric Reduction of Ketones Using Organometallic Catalysts 330 $aCatalysts are increasingly used by chemists engaged in fine chemical synthesis within both industry and academia. Today, there exists a huge choice of high-tech catalysts, which add enormously to the repertoire of synthetic possibilities. However, catalysts are occasionally capricious, sometimes difficult to use and almost always require both skill and experience in order to achieve optimal results. This series aims to be a practical help for advanced undergraduate, graduate and postgraduate students, as well as experienced chemists in industry and academia working in organic and organometalli 410 0$aCatalysts For Fine Chemicals Synthesis 606 $aCatalysts 606 $aChemistry, Organic 606 $aChemistry, Organic 606 $aEnzymes 606 $aHydrolysis 606 $aOrganic compounds 606 $aOxidation-reduction reaction 606 $aSynthesis 606 $aBiomedical Engineering$2HILCC 606 $aHealth & Biological Sciences$2HILCC 615 4$aCatalysts. 615 4$aChemistry, Organic. 615 4$aChemistry, Organic. 615 4$aEnzymes. 615 4$aHydrolysis. 615 4$aOrganic compounds. 615 4$aOxidation-reduction reaction. 615 4$aSynthesis. 615 7$aBiomedical Engineering 615 7$aHealth & Biological Sciences 676 $a660.634 676 $a660/.28443 700 $aRoberts$b Stanley M$0754844 701 $aPoignant$b Geraldine$043932 801 0$bAU-PeEL 801 1$bAU-PeEL 801 2$bAU-PeEL 906 $aBOOK 912 $a996218171503316 996 $aCatalysts for Fine Chemical Synthesis$92041353 997 $aUNISA LEADER 01788nam0 22004093i 450 001 NAP0426463 005 20251003044251.0 010 $a1563966255 100 $a20090121d1996 ||||0itac50 ba 101 | $aeng 102 $aus 181 1$6z01$ai $bxxxe 182 1$6z01$an 200 1 $aSpace charge dominated beams and applications of high brightness beams$eBloomington, IN, October 10-13, 1995$feditor S. Y. Lee 210 $aWoodbury (N.Y.)$cAIP press$dc1996 215 $aXIX, 522 p.$cill.$d24 cm. 225 | $aAIP conference proceedings$v377 410 0$1001RAV0031237$12001 $aAIP conference proceedings$v377 606 $aAcceleratori di particelle$xCongressi$x1995$2FIR$3NAPC235477$9I 676 $a539.7$9Fisica atomica e nucleare$v14 676 $a539.73$9Fisica atomica e nucleare. Accelerazione di particelle$v20 696 $aConvegni$aCongressi e convegni$aMacchine acceleratrici di particelle$aAcceleratori nucleari$aAcceleratori 699 $aCongressi$yConvegni 699 $aCongressi$yCongressi e convegni 699 $aAcceleratori di particelle$yMacchine acceleratrici di particelle 699 $aAcceleratori di particelle$zAcceleratori nucleari 699 $aAcceleratori di particelle$zAcceleratori 702 1$aLee$b, S. Y.$3UFIV149273 790 1$aLee$b, Shyh-Yuan$3SBNV069316$zLee, S. Y. 801 3$aIT$bIT-000000$c20090121 850 $aIT-BN0095 901 $bNAP 01$cSALA DING $n$ 912 $aNAP0426463 950 0$aBiblioteca Centralizzata di Ateneo$c1 v.$d 01SALA DING 539.7 SPACDB$e 0102 0000040345 VMA 1 v.$fY $h20020313$i20020313 977 $a 01 996 $aSpace charge dominated beams and applications of high brightness beams$91573174 997 $aUNISANNIO