TY - BOOK AU - AU - Ratovelomanana-Vidal,Virginie AU - Phansavath,Phannarath TI - Asymmetric hydrogenation and transfer hydrogenation = SN - 9783527822300 AV - QD281.H8 U1 - 547/.23 23 PY - 2021///] CY - Hoboken, New Jersey PB - Wiley KW - Hydrogenation KW - Hydrog�enation KW - Biochemistry KW - bisacsh/2022 KW - Life Sciences KW - SCIENCE KW - bisacsh/2023 KW - bisacsh/2024 KW - fast KW - Electronic books N1 - Includes bibliographical references and index; 7.3.1.2 Reduction Under Aqueous Conditions -- 7.3.1.3 Hydrogenation with Hydrogen Gas -- 7.3.1.4 Racemic Catalysts for Reductions -- 7.3.1.5 Specific Applications to Complex Acetophenone Derivatives -- 7.3.2 Reductions of Acetylenic Ketones -- 7.3.3 Reductions of Benzophenone Ketones -- 7.3.4 Reductions of Diverse Ketones -- 7.3.5 Dynamic Kinetic Resolutions -- 7.3.6 Reductions of Imines -- 7.4 Conclusions and Outlook -- References -- Chapter 8 Homogeneous Asymmetric Hydrogenation of Heteroaromatic Compounds Catalyzed by Transition Metal Complexes -- 8.1 Introduction -- 8.2 Asymmetric Hydrogenation of Quinolines -- 8.3 Asymmetric Hydrogenation of Quinoxalines -- 8.4 Asymmetric Hydrogenation of Isoquinolines -- 8.5 Asymmetric Hydrogenation of Pyridines and Pyrazines -- 8.6 Asymmetric Hydrogenation of Indoles and Pyrroles -- 8.7 Asymmetric Hydrogenation of Heteroarenes with Multi-N-Heterocycles -- 8.8 Asymmetric Hydrogenation of Other N-Heteroarenes -- 8.9 Asymmetric Hydrogenation of O- and S-Heteroarenes -- 8.10 Summary and Conclusions -- Acknowledgments -- References -- Chapter 9 Asymmetric (Transfer) Hydrogenation of Imines -- 9.1 Asymmetric Hydrogenation of Imines -- 9.1.1 Iridium Catalysts -- 9.1.1.1 (P,P) Ligands -- 9.1.1.2 (P,N) Ligands -- 9.1.1.3 P-Monodentate Ligands -- 9.1.2 Rhodium and Palladium Catalysts -- 9.2 Asymmetric Transfer Hydrogenation of Imines -- 9.2.1 Ruthenium Catalysts -- 9.2.2 Iridium and Rhodium Catalysts -- 9.2.3 Iron Catalysts -- 9.3 New Approaches -- 9.3.1 Metal Free -- 9.3.2 Biocatalytic Imine Reduction -- 9.3.2.1 Artificial Metalloenzymes -- 9.3.2.2 Imine Reductases (IREDs) -- 9.4 Summary and Conclusions -- References -- Chapter 10 Asymmetric Hydrogenation in Continuous-Flow Conditions -- 10.1 Introduction -- 10.2 Chirally Modified Metal Surfaces -- 10.3 Well-defined Transition-metal Complexes; 10.3.1 Immobilized Systems -- 10.3.1.1 Covalently Anchored Ligands -- 10.3.1.2 Immobilization by the Augustine Method -- 10.3.1.3 Ionic Liquids as Matrices for Transition-metal Complex Catalysts -- 10.3.2 Homogeneous Systems -- 10.3.3 Self-supported Systems -- 10.4 Organocatalysts -- 10.5 Chiral Auxiliary-controlled Asymmetric Hydrogenation in Flow -- 10.6 Summary and Outlook -- References -- Chapter 11 Organocatalytic Asymmetric Transfer Hydrogenation Reactions -- 11.1 Introduction -- 11.2 Reduction of C C Double Bonds -- 11.3 Reduction of C N Double Bonds -- 11.4 Cascade Reactions -- 11.5 Dearomatization -- 11.6 Conclusions -- References -- Index -- EULA N2 - "The development of efficient and straightforward methods to obtain chiral compounds is an important and challenging research area in modern synthetic organic chemistry. Especially asymmetric hydrogenation reactions have been investigated extensively in the past decades. This reaction methodology was pioneered by Knowles and Noyori (Nobel Prize in Chemistry 2001) and is now frequently used in both academia and industry. It is an economical reaction, easy to carry out, and environmentally friendly. It allows the efficient preparation of chiral building blocks of natural products, pharmaceuticals, agrochemicals, and flavors"-- UR - http://www.vlebooks.com/vleweb/product/openreader?id=none&isbn=9783527822317 UR - https://ebook.yourcloudlibrary.com/library/oclc/detail/6q584z9 UR - https://images.yourcloudlibrary.com/delivery/img?type=DOCUMENTIMAGE&documentID=6q584z9&size=LARGE UR - https://images.yourcloudlibrary.com/delivery/img?type=DOCUMENTIMAGE&documentID=6q584z9&size=ORIGINAL UR - https://images.yourcloudlibrary.com/delivery/img?type=DOCUMENTIMAGE&documentID=6q584z9&size=MEDIUM UR - https://app.kortext.com/borrow/925438 UR - https://www.hoopladigital.com/title/14889222?utm_source=MARC&Lid=hh4572 UR - https://d2snwnmzyr8jue.cloudfront.net/jws_9783527822300_180.jpeg ER -