000 06367cam a22007458i 4500
001 33960
003 OCoLC
005 20250805131534.0
006 m o d
007 cr |||||||||||
008 200604s2021 nju ob 001 0 eng
010 _a 2020025501
020 _a9783527822300
_q(epub)
020 _a9783527346103
020 _a9783527822317
_q(adobe pdf)
020 _a3527822313
020 _z9783527346103
_q(hardback)
035 _a(OCoLC)1158506562
_z(OCoLC)1245420899
040 _aDLC
_beng
_erda
_cDLC
042 _apcc
050 0 0 _aQD281.H8
082 0 0 _a547/.23
_223
100 _qRatovelomanana-Vidal
_eaurther
245 0 0 _aAsymmetric hydrogenation and transfer hydrogenation =
_cedited by Virginie Ratovelomanana-Vidal, Phannarath Phansavath.
250 _aFirst edition.
263 _a2008
264 1 _aHoboken, New Jersey :
_bWiley,
_c[2021]
300 _a384 paper
_bمعادلات ورسوم
_c24
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bn
_2rdamedia
338 _aonline resource
_bnc
_2rdacarrier
504 _aIncludes bibliographical references and index.
505 8 _a7.3.1.2 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.
505 8 _a10.3.1 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.
520 _a"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"--
588 _aDescription based on print version record and CIP data provided by publisher; resource not viewed.
650 0 _aHydrogenation.
650 2 _aHydrogenation
650 6 _aHydrog�enation.
650 7 _aBiochemistry.
_2bisacsh/2022
650 7 _aLife Sciences.
_2bisacsh/2022
650 7 _aSCIENCE.
_2bisacsh/2022
650 7 _aBiochemistry.
_2bisacsh/2023
650 7 _aLife Sciences.
_2bisacsh/2023
650 7 _aSCIENCE.
_2bisacsh/2023
650 7 _aBiochemistry.
_2bisacsh/2024
650 7 _aLife Sciences.
_2bisacsh/2024
650 7 _aSCIENCE.
_2bisacsh/2024
650 7 _aHydrogenation
_2fast
655 0 _aElectronic books.
700 1 _aRatovelomanana-Vidal, Virginie,
_eeditor.
700 1 _aPhansavath, Phannarath,
_eeditor.
776 0 8 _iPrint version:
_tAsymmetric hydrogenation and transfer hydrogenation
_bFirst edition.
_dHoboken, New Jersey : Wiley, [2021]
_z9783527346103
_w(DLC) 2020025500
856 4 0 _uhttp://www.vlebooks.com/vleweb/product/openreader?id=none&isbn=9783527822317
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910 _aمها ازاد حامد
942 _2ddc
_cBK
948 _hNO HOLDINGS IN IQMCL - 14 OTHER HOLDINGS
999 _c33960
_d33960