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Lewis Base Catalysis in Organic Synthesis

1. Aufl.

von: Edwin Vedejs, Scott E. Denmark
457,99 €
Verlag:	Wiley-VCH
Format:	EPUB
Veröffentl.:	03.08.2016
ISBN/EAN:	9783527675173
Sprache:	englisch
Anzahl Seiten:	1488

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Beschreibungen

Titelbeschreibung

This three-volume set represents the first comprehensive coverage of the rapidly expanding field of Lewis base catalysis that has attracted enormous attention in recent years. Lewis base catalysis is a conceptually novel paradigm that encompasses an extremely wide variety of preparatively useful transformations and is particularly effective for enantioselectively constructing new stereogenic centers. As electron-pair donors, Lewis bases can influence the rate and stereochemical course of myriad synthetic organic reactions. The book presents the conceptual/mechanistic principles that underlie Lewis base catalysis, and then builds upon that foundation with a thorough presentation of many different reaction types. And last but not least, the editors, Prof. Edwin Vedejs and Prof. Scott E. Denmark, are without doubt the leaders in this emerging field and have compiled high quality contributions from an impressive collection of international experts.

Inhaltsverzeichnis

Preface for Volumes 1–3 XV Introduction: Definitions of Catalysis XXI Volume 1 1 From Catalysis to Lewis Base Catalysis with Highlights from 1806 to 1970 1 Edwin Vedejs 1.1 Introduction 1 1.2 Catalysis 1 1.3 Progress with Catalysis in Organic Chemistry 3 1.4 Ostwald’s Redefinition of Catalysis 5 1.5 The First Example of Lewis Base Catalysis 7 1.6 The Road to Mechanistic Comprehension; Multistage Catalysis by Lewis Base 9 1.7 An Uneven Path to a Unifying Concept 12 1.8 Amine Catalysis 17 1.9 Summary 26 Section I Principles 31 2 Principles, Definitions, Terminology, and Orbital Analysis of Lewis Base–Lewis Acid Interactions Leading to Catalysis 33 Scott E. Denmark and Gregory L. Beutner 2.1 Introduction 33 2.2 Lewis Definitions of Valence and the Chemical Bond 34 2.3 Extensions, Expansions of, and Objections to the Lewis Definitions 35 2.4 Interpretation of the Lewis Definitions in the Idiom of Molecular Orbital Theory and Quantum Mechanics 38 2.5 Defining Lewis Base Catalysis 40 2.6 Theoretical Analysis of the Geometrical and Electronic Consequences of Lewis Acid–Lewis Base Interactions 44 2.7 Summary 51 3 Thermodynamic Treatments of Lewis Basicity 55 Jean-François Gal 3.1 Introduction 55 3.2 Basic Thermodynamics for the Study of Lewis Acid–Base Interactions 56 3.3 Scales of Lewis Affinity and Basicity 58 3.4 Lewis Acidity and Lewis Basicity: Thermodynamic Scales 62 3.5 Quantum Chemical Tools 74 3.6 Conclusion and Overview 75 3.7 Summary 76 List of Abbreviations 77 4 Quantitative Treatments of Nucleophilicity and Carbon Lewis Basicity 85 Sami Lakhdar 4.1 Introduction 85 4.2 Nucleophilicity 85 4.3 Lewis Basicity 91 4.4 Nucleofugality 93 4.5 Selected Applications 95 4.6 Conclusion 113 4.7 Summary 113 Section II Mechanism and Lewis Base Catalysis: Nucleophilicity Is Only Part of the Story 119 5 Anhydride Activation by 4-Dialkylaminopyridines and Analogs 121 Raman Tandon and Hendrik Zipse 5.1 Historical Background 121 5.2 Mechanistic Considerations 121 5.3 Catalyst Structure and Variation 124 5.4 The Influence of Reaction Conditions 130 5.5 The Influence of Acyl Donors 132 5.6 The Influence of Substrate Structure 136 5.7 Summary 141 6 Mechanistic Understanding of Proline Analogs and Related Protic Lewis Bases 145 Alan Armstrong and Paul Dingwall 6.1 Proline Catalysis: Overview 145 6.2 Mechanism of the Proline-Catalyzed Aldol Reaction 147 6.3 Mechanism of the Proline-Catalyzed α-Amination and α-Aminoxylation Reactions 161 6.4 The Proline-Mediated Conjugate Addition Reaction 170 6.5 Modified Proline Derivatives 175 6.6 Concluding Remarks 186 7 Mechanistic Options for the Morita–Baylis–Hillman Reaction 191 Marilia S. Santos, José Tiago M. Correia, Ana Paula L. Batista, Manoel T. Rodrigues Jr., Ataualpa A. C. Braga, Marcos N. Eberlin, and Fernando Coelho 7.1 The Morita–Baylis–Hillman Reaction: An Overview 191 7.2 Kinetic Studies Applied to aza-Morita–Baylis–Hillman Reaction 195 7.3 Theoretical Calculations Applied to MBH Reaction 208 7.4 Mass Spectrometry Aid the Understanding of the Morita–Baylis–Hillman Reaction 217 7.5 Classical and Nonclassical Methods for Mechanistic Studies Associated with the Morita–Baylis–Hillman Reaction: Which Is the Correct Pathway of This Reaction? 226 8 Mechanism of C-Si Bond Cleavage Using Lewis Bases 233 Hans J. Reich 8.1 Introduction 233 8.2 Mechanistic Issues 235 8.3 Alkylation 247 8.4 Benzylation 253 8.5 Allylation 255 8.6 Allenylation/Propargylation 260 8.7 Alkynylation 261 8.8 Arylation 262 8.9 Vinylation 263 8.10 Cyanation 264 8.11 Summary 275 9 Bifunctional Lewis Base Catalysis with Dual Activation of X3Si-Nu and C=)O 281 9.1 Addition of Allyltrichlorosilanes to Aldehydes 281 9.2 Aldol Additions of Trichlorosilyl Enol Ethers Derived from Ketones, Aldehydes, and Esters 293 10 Bifunctional Lewis Base Catalysis with Dual Activation of R–M and C=O 339 10.1 Introduction 339 10.2 Activation of C–Zn and Related C–Mg by a Simple Lewis Base 340 10.3 Lewis Base-Activated C–Zn + C 10.4 Role of Dimeric Organozinc Species 345 10.5 Scope of Carbonyl Substrates in Catalytic Asymmetric Organozinc Addition Reaction 350 10.6 Anionic Lewis Base Activation in Mg(II) and Zn(II) Ate Complexes 372 10.7 Summary 382 11 The Corey–Bakshi–Shibata Reduction: Mechanistic and Synthetic Considerations – Bifunctional Lewis Base Catalysis with Dual Activation 387 Christopher J. Helal and Matthew P. Meyer 11.1 Introduction 387 11.2 The Catalytic Cycle 389 11.3 Mechanism 393 11.4 Applications of the CBS Reduction in Organic Synthesis 416 Volume 2 Section III Applications: Lewis Base Catalysis Involving an Activation Step 457 12 Chiral Lewis Base Activation of Acyl and Related Donors in Enantioselective Transformations 459 James I. Murray, Zsofia Heckenast, and Alan C. Spivey 13 Catalytic Generation of Ammonium Enolates and Related Tertiary Amine-Derived Intermediates: Applications, Mechanism, and Stereochemical Models 527 Khoi N. Van, Louis C. Morrill, Andrew D. Smith, and Daniel Romo 14 Morita–Baylis–Hillman, Vinylogous Morita–Baylis–Hillman, and Rauhut–Currier Reactions 655 Allison M. Wensley, Nolan T. McDougal, and Scott E. Schaus 15 Beyond the Morita–Baylis–Hilman Reaction 715 Yi Chiao Fan and Ohyun Kwon 16 Iminium Catalysis 805 Aurélie Claraz, Juha H. Siitonen, and Petri M. Pihko 17 Enamine-Mediated Catalysis 857 John J. Murphy, Mattia Silvi, and Paolo Melchiorre Volume 3 Section IVa Applications: Enhanced Nucleophilicity by Lewis Base Activation 903 18 Si-C-X and Si-C-EWG as Carbanion Equivalents under Lewis Base Activation 905 Ping Fang, Chang-Hua Ding, and Xue-Long Hou 19 Activation of B-B and B-Si Bonds and Synthesis of Organoboron and Organosilicon Compounds through Lewis Base-Catalyzed Transformations 967 Amir H. Hoveyda, Hao Wu, Suttipol Radomkit, Jeannette M. Garcia, Fredrik Haeffner, and Kang-sang Lee Section IVb Applications: Enhanced Electrophilicity and Dual Activation by Lewis Base Catalysis 1011 20 Lewis Base-Catalyzed Reactions of SiX3-Based Reagents with C 21 Lewis Base-Catalyzed, Lewis Acid-Mediated Reactions 1039 Sergio Rossi and Scott E. Denmark 22 Lewis Bases as Catalysts in the Reduction of Imines and Ketones with Silanes 1077 Pavel Kočovský and Andrei V. Malkov 23 Reactions of Epoxides 1113 Tyler W. Wilson and Scott E. Denmark Section V Lewis Base-Catalyzed Generation of Electrophilic Intermediates 1153 24 Lewis Base Catalysis: A Platform for Enantioselective Addition to Alkenes Using Group 16 and 17 Lewis Acids 1155 Dipannita Kalyani, David J.-P. Kornfilt, Matthew T. Burk, and Scott E. Denmark Section VI Bifunctional (and Multifunctional) Catalysis 1213 25 Bifunctional and Synergistic Catalysis: Lewis Acid Catalysis and Lewis Base-Assisted Bond Polarization 1215 Won-jin Chung and Scott E. Denmark 26 Bifunctional Catalysis with Lewis Base and X-H Sites That Facilitate Proton Transfer or Hydrogen Bonding 1259 Curren T. Mbofana and Scott J. Miller Section VII Carbenes: Lewis Base Catalysis Triggers Multiple Activation Pathways 1289 27 Catalysis with Stable Carbenes 1291 Darrin M. Flanigan, Nicholas A. White, Kevin M. Oberg, and Tomislav Rovis Summation 1351 Index 1355

Autorenportrait

Edwin Vedejs was born in 1941 in Riga, Latvia. After completion of his BS (University of Michigan, 1962) and PhD (University of Wisconsin, 1966), he spent a postdoctoral year with E. J. Corey at Harvard. Prof. Vedejs then joined the chemistry faculty at the University of Wisconsin (1967). In 1999, he returned to the University of Michigan as the Moses Gomberg Professor of Chemistry. Work in the Vedejs group combines topics at the interface of methodology, total synthesis, heterocycle chemistry, stereochemistry, and related mechanistic studies. Prof. Vedejs has won several awards: Alexander von Humboldt Senior Scientist Award, 1984; Professore a Contratto, University of Bologna, Italy, 1988; Helfaer Professor, 1991-1996 (UW); Pharmacia&Upjohn Teaching Award, 1996 (Chemistry Dept, UW). Robert M. Bock Professor (UW), 1997-98; Paul Walden Medal, Riga Technical University (1997); H. C. Brown Award for Creative Research in Synthetic Methods, 2004 (ACS). Grand Medal of the Latvian Academy of Sciences, 2005. Order of the Three Stars, Latvia, 2006. Honorary Doctorate, Riga Technical University 2010. Scott E. Denmark was born in New York on 17 June 1953. He obtained an S. B. degree from M.I.T. in 1975 and a D. Sc. Tech degree in 1980 from the ETH-Zürich under the direction of Professor Albert Eschenmoser. That same year he began his career as assistant professor at the University of Illinois. He was promoted to associate professor in 1986, full professor in 1987 and then in 1991 named the Reynold C. Fuson Professor of Chemistry. Professor Denmark?s research interests focus on the invention of new synthetic reactions and elucidating the origins of stereocontrol in novel, asymmetric transformations. He has pioneered the concept of chiral Lewis base activation of Lewis acids for catalysis in main group chemistry. His group has also developed palladium-catalyzed cross-couplings with organofunctional silicon compounds. In addition he is well-known for the development and application of tandem cycloadditions of nitroalkenes for the synthesis of complex natural and unnatural nitrogen containing compounds. In recent years, his group has investigated the use of chemoinformatics to identify and optimize catalysts for a variety of organic and organometallic reactions. Professor Denmark has won a number of honors for both research and teaching including: an NSF Presidential Young Investigator Award, A. C. Cope Scholar Award (ACS), Alexander von Humboldt Senior Scientist Award, Pedler Lecture and Medal (RSC), the ACS Award for Creative Work in Synthetic Organic Chemistry, the Yamada-Koga Prize, the Prelog Medal (ETH-Zürich), the H. C. Brown Award for Creative Research in Synthetic Methods (ACS), Robert Robinson Lecture and Medal (RSC), the ISHC Senior Award in Heterocyclic Chemistry, Paul Karrer Lectureship (Uni Zürich), the Frederic Stanley Kipping Award for Research in Silicon Chemistry (ACS), and the Harry and Carol Mosher Award (Santa Clara Section, ACS). He is a Fellow of the Royal Society of Chemistry and the American Chemical Society. He edited Volume 85 of Organic Syntheses, was Editor of Volumes 22-25 of Topics in Stereochemistry and was a founding Associate Editor of Organic Letters (1999-2004). After serving on the editorial board from 1994-2003, he became Editor in Chief and President of Organic Reactions, Inc. in 2008.