Page 233 - Catalysts for Fine Chemical Synthesis Vol 1 - Robert & Poignant

222 index

diazo-ester 37 a,b-unsaturated carbonyl
1,1 -di(benzoyl)ferrocene, synthesis compounds 55±69
0
202±3 a,b-unsaturated esters 87±102
di-tert butyl 2,2-dimethylmalonate 31 epoxy alcohol 20
Diels±Alder reaction 30, 32, 33 a,b-epoxy ketones 65
diethyl tartrate 19 Escherichia coli 28
diethylzinc 65 Escherichia coli JM109 17
chiral modified 61±2 esters
(R,R)-1,2- epoxidation 87±102
dihydroxycyclohexyl)acetonitrile hydrolysis 4±9
acetonide 107±8 Et 2 AlCl 31
(‡)-diisopropyl tartrate 21 ethyl 4-acetamido-3-oxo-5-phenyl-4-
dimethyl itaconate, hydrogenation 177±8 pentenoate, asymmetric
E-dioxoruthenium(VI) complexes, hydrogenation 214±17
preparation 98±9 ethyl (Z)-4-acetamido-3-oxo-5-phenyl-4-
disubstituted E-alkenes 87 pentenoate, synthesis 213±14
asymmetric epoxidation 94±8 ethyl aluminium dichloride 30
disubstituted Z-alkenes 87 (Z)-ethyl cinnamate, epoxidation 91±2
asymmetric epoxidation 88±93 ethyl-3-oxobutanoate 12
b,b-disubstituted enamides, ethyl (1S,3R,4R)-2-[(S)-1-
hydrogenation 181 phenylethylamino]-2-
DuPHOS 16 azabicyclo[2.2.1] hept-5-ene-3-
carboxylate, synthesis 129±31
a-enamides, asymmetric
hydrogenation 176 functionalized carbohydrates 22
enantioselective epoxidation, (E)-b- furylhydroperoxides 111
methylstyrene 98±101
enantioselective reduction of ketones, galactosyltransferase 38
using N-arylsulfonyl gas chromatography (GC) 49
oxazaborolidines 166±8 Genkt modification 120
enantioselective Rh-catalysed preparation geraniol 14
of chiral a-amino acids 202±10
enantioselective Ru-catalyzed hapten 34
hydrogenation of vinylphosphonic Hevea brasiliensis 27
acids 190±4 (E)-2-hexen-1-ol, epoxidation 78±80
enantioselective synthesis of (Z)-N- high pressure liquid chromatography
carbobenzyloxy-3-hydroxyproline (HPLC) 49
ethylester 140±2 homoallylic alcohols, oxidation 84
enol carbonates, hydrogenation 186±9 HSi(OEt) 3 171
enol silanes 28 hydrocyanation, alkenes 35
enones, epoxidation 61 hydrogen transfer reduction of
epoxidation ketones 134
(E)-2-alkyliden-1-oxo-1,2,3,4- hydrogenation
tetrahydronaphthalenes 65 a-amidoacrylate 179±86
allylic alcohols 71±86 b,b-disubstituted enamides 181
cinnamyl alcohol 74±6 carbonyl compounds 118
enones 61 dimethyl itaconate 177±8
(Z)-ethyl cinnamate 91±2 enol carbonates and 4-methylene-N-
(E)-2-hexen-1-ol 78±80 acyloxazolidinone 186±9
2-isobutylidene-1-tetralone 62±3 hydrogenation reaction, scope 193±4
(E)-2-methyl-3-phenyl-2-propenol b-hydroxy-a-amino acid derivatives 28
76±8 (R)-3-hydroxyester 13
(Z)-methyl styrene 89±90 (S)-hydroxyester 12
unfunctionalized alkenes 87±102 (R)-5-hydroxyhexanoic acid 10