Page 234 - Catalysts for Fine Chemical Synthesis Vol 1 - Robert & Poignant
P. 234

index                            223

             (1S,3R,4R)-3-hydroxymethyl-2-     (S)-2-methyl-2,3-butanediol,
                azabicyclo[2.2.1]heptane,          synthesis  187±8
                sythesis  131±2                (R)-(ÿ)-methyl-3-hydroxypentanoate,
             6-hydroxynicotinic acid 17            synthesis  126±7
             (R)-2-(4-hydroxyphenoxy)propanoic  methyl-3-oxobutanoate  13
                acid  17                       methyl-3-oxo-2-trityloxyiminostearate,
             b-hydroxysulfoxamine borane,          stereoselective reduction  163±4
                preparation  151±3             (E)-2-methyl-3-phenyl-2-propenol,
             hydroxysulfoximines  12               epoxidation 76±8
                                               (Z)-methyl styrene, epoxidation 89±90
             2-isobutylidene-1-tetralone,      methyl para-tolyl sulfide  25
                epoxidation  62±3                oxidation  26
                                               4-methylene-N-acyloxazolidinone,
             Katsuki±Sharpless oxidation 20, 21    hydrogenation  186±9
             keto esters, asymmetric           methylene chloride  15
                hydrogenation  128             (1R,2R)-N-methylpseudoephedrine  65
             b-keto esters, asymmetric         (E)-b-methylstyrene  22
                hydrogenation  121±3             enantioselective epoxidation 99±101
             ketones  22, 23                   methylsulfides,asymmetricoxidation 110
               asymmetric hydrogenation  115±36  morphinans 14
               asymmetric reduction  148       Mosher esters, preparation  171
               enantioselective reduction using  MTPA chloride, derivatization with 75±6
                  N-arylsulfonyl               Mucor sp.  17
                  oxazaborolidines 166±8       Mukaiyama coupling  28
               hydrogen transfer reduction  134
               reduction by borane catalysts  145  NaHCO 3  22
               reduction using amino acid anions as  NaOH  34
                  catalyst and hydrosilane as  naphthyl constituent  192±3
                  oxidant 169±72               naproxen precursor  36
             kinetic resolution of racemic     [NH 2 (C 2 H 5 ) 2 ]  13
                4-bromophenyl methyl           nickel±DIOP system  35
                sulfoxide  111±13              Ni(COD) 2  35
             kinetic resolution of sulfoxides  109±13  nitriles, hydrolysis 4±9
                                               non-asymmetric epoxidation 55±6
             La-(R)-BINOL-Ph 3 PO/cumene         allylic alcohols  72±3
                hydroperoxide system  66±9     nonmetallic catalysts
             Lactobacillus sp. 11                asymmetric reduction using  143±73
             lanthanoid±BINOL complexes  23      reduction by  156
             leucine N-carboxyanhydride,       nonracemic chiral epoxides 51
                synthesis  57±8
                                               n-octane 7
             maleimide  31                     olefin hydrogenation by transition metal
             manganese(III) complex  88            complexes  177
             manganese±salen complex  21       organometallic catalysts  175±212
             Manihot esculenta 27              oxabicyclooctene  34
             (S)-Me-CBS  148                   oxazaborolidine borane reduction of
             MeCN 3 Mo(CO) 3  37                   acetophenone 146±8
             (Me 3 CO 2 C) 2 CMe 2  31         oxazaborolidines  32
             menthol  30                       oxazaphosphinamide borane reduction of
             metal-catalysed reduction             chloroacetophenone  148±50
                mechanism  118                 oxazaphosphinamides  12
             methacrolein  31                  oxidation
             4-methoxystryrene, asymmetric       (Z)-allylic alcohols  84
                aminohydroxylation  103±5        homoallylic alcohols  84
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