Page 6 - Catalysts for Fine Chemical Synthesis Vol 1 - Robert & Poignant
P. 6

Contents









             Series Preface . . . . . . . . . . . . . . . . . . . .          xiii

             Preface to Volume 1 . . . . . . . . . . . . . . . . . .          xv

             Abbreviations . . . . . . . . . . . . . . . . . . . .           xvii

                     ev
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                       iew
             Part I: Review  . . . . . . . . . . . . . . . . . . .             1
                    R
                  I:
             1  The Integration of Biotransformations into the
                Catalyst Portfolio  . . . . . . . . . . . . . . . . .          3
                1.1  Hydrolysis of esters, amides, nitriles and
                    oxiranes . . . . . . . . . . . . . . . . . . . .           4
                1.2  Reduction reactions . . . . . . . . . . . . . . . .       9
                    1.2.1  Reduction of carbonyl compounds . . . . . . .      10
                    1.2.2  Reduction of alkenes . . . . . . . . . . . .       13
                1.3  Oxidative transformations . . . . . . . . . . . . .      17
                1.4  Carbon±carbon bond-forming reactions . . . . . . . .     26
                1.5  Conclusions . . . . . . . . . . . . . . . . . . .        37
                References . . . . . . . . . . . . . . . . . . . . .          39


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                  II:
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             Part II: Procedures . . . . . . . . . . . . . . . . .     .      47
             2  General Information. . . . . . . . . . . . . . . . .          49
             3  Asymmetric Epoxidation . . . . . . . . . . . . . . .          51
                3.1  Introduction. . . . . . . . . . . . . . . . . . .        51
                References . . . . . . . . . . . . . . . . . . . . .          52
             4  Epoxidation of a, b-Unsaturated Carbonyl Compounds . . . .    55
                4.1  Non-asymmetric epoxidation . . . . . . . . . . . .       55
                4.2  Asymmetric epoxidation using poly-d-leucine . . . . . .  56
                    4.2.1  Synthesis of leucine N-carboxyanhydride . . . . .  57
                    4.2.2  Synthesis of immobilized poly-d-leucine . . . . .  58
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