Page 235 - Catalysts for Fine Chemical Synthesis Vol 1 - Robert & Poignant
P. 235

224                            index

               oxidative transformations  17±26     by nonmetallic catalysts  156
               oxiranes, hydrolysis  4±9            carbonyl, by borane 144
               5-oxohexanoic acid  10               carbonyl compounds  10±13
               oxone  22                            chloroacetophenone, using sulfoxamine
                                                       borane 153±5
               Pd(PPh 3 ) 4  37                     dialkylketones  11
               pentane-2,4-dione  13                ketones
               (R,R)-2,4-pentanediol  13              by borane catalysts 145
               3-phenylcyclobutanone  24              using amino acid anions as catalyst
               phosphino-oxazoline copper(II)          and hydrosilane as oxidant
                   complex  33                         169±72
               Pichia farinosa  14                  metal-catalysed mechanism  118
               pig liver esterase (ple)  5          oxazaphosphinamide  148±50
               pivaldehyde  25                      reactions  9±16
               polyamino acids 24                   see also asymmetric reduction;
               polyclonal antibody  34                 enantioselective reduction;
               poly-D-leucine                          hydrogen transfer reduction;
                 asymmetric epoxidation using 56±61    stereoselective reduction
                 synthesis  58±9                  [Rh((R)-BiNAP)] complexes  186±9
               poly-D-leucine catalyst 56         Rh(B[3.2.0]DPO) complexes  180±6
               poly-L-leucine  24, 61               a-acetamido cinnamic acid reduction
               poly(octamethylene tartrate)  84        by 185
               poly(octamethylene-L-(‡)-tartrate,  Rh-catalyzed asymmetric hydrogenation
                   synthesis 81±2                    of a-(acylamino)acrylic acids and
               poly(tartrate)  84                    esters  202
               porcine pancreatic lipase  6       Rh±DuPHOS   16
               potassium caroate  22              Rh(I)±BINAPHOS   35
               potassium ferricyanide  18         Rh(I) catalysts, asymmetric
               potassium peroxomonosulfate  51       hydrogenation using  213±17
               progesterone, hydroxylation  17    Rh(I) complexes  35
               proline  172                       Rhizopus sp.  17
               (R)-N-propionyl-4,5,5-trimethyl-   [Rh((S,S)-Me-BPE)]  177±8
                   1,3-oxazolidine-2-one, synthesis  189  [Rh((R,R)-Me-DuPHOS)]  179±80
               N-(2-pryidinesulfonyl)-1-amino-2-  Rhodococcus erthyrolpolis  8
                   indanol  169                   Rhodococcus sp. SP361 9
               Pseudomonas cepacia lipase  6      Ru(II)-(2-azanorbornyl-methanol)
               Pseudomonas fluorescens lipase  6, 7   complexes  129, 134
               Pseudomonas putida  5              Ru±BINAP   13, 14, 15, 117±21
               N-(2-pyridinesulfonyl)-1-amino-2-  Ru(II)-catalysed asymmetric
                   indanol, synthesis  166±7          hydrogenation  15
                                                  Ru(II) catalysts  192±3
               racemic 4-bromophenyl methyl sulfoxide,  asymmetric hydrogenation using
                   kinetic resolution  111±13          213±17
               RAMA    28                         Ru(II) porphyric 101
               recrystallization of 2-bromo-(3-nitro-4-  Ru(S)±tetrahydroBINAP  15
                   benzyloxyphenyl)ethanol 158±61
               reduction                          Saccharomyses sp.  12
                 a-acetamido cinnamic acid, by    salen±manganese complexes  88±93
                     rhodium (B[3.2.0]DPO)        Schlenk tube  119±20
                     complexes  185               sialyl Lewis tetrasaccharide 38
                 acetophenone, by oxazaborolidine  sodium hypochlorite  21
                     borane 146±8                 stereoselective reduction
                 alkenes  13±16                     2,3-butadione monoxime trityl
                 alkylaryl ketones  11                 ether 161±2
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