Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules

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1. Verfasser: Vicario, Jose L. (VerfasserIn)
Format: Buch
Sprache:English
Veröffentlicht: Cambridge RSC Publ. 2010
Schriftenreihe:RSC catalysis series 5
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Datensatz im Suchindex

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adam_text Titel: Organocatalytic enantioselective conjugate addition reactions Autor: Vicario, Jose L Jahr: 2010 Contents Chapter 1 Introduction 1 1.1 Organocatalysis: an Emerging Field 1 1.2 Historical Evolution of Asymmetrie Organocatalysis 5 1.3 Types of Organocatalysts 9 1.4 The Conjugate Addition Reaction: a Very Convenient Platform for Asymmetrie Organocatalysis 11 1.5 On the Organization of This Book 12 References and Notes 13 Chapter 2 Enantioselective Conjugate Addition Reactions via Enamine Activation 18 2.1 Introduction 18 2.1.1 Factors Influencing the Stereocontrol in Michael Additions Proceeding via Enamine Activation 20 2.2 Nitroalkenes as Michael Acceptors 23 2.2.1 Ketones as Michael Donors 23 2.2.2 Aldehydes as Michael Donors 33 2.2.3 Reactions under Non-conventional Methodologies 42 2.3 Enones and Enals as Michael Acceptors 45 2.4 Doubly Activated Olefins as Michael Acceptors 50 2.5 Concluding Remarks 56 References and Notes 56 RSC Catalysis Series No. 5 Organocatalytic Enantioselective Conjugate Addition Reactions: A Powerful Tool for the Stereocontrolled Synthesis of Complex Molecules By Jose L. Vicario, Dolores Badia, Luisa Carriüo and Efraim Reyes © J. L. Vicario, D. Badia, L. Carrillo and E. Reyes 2010 Published by the Royal Society of Chemistry, www.rsc.org viü Contents Chapter 3 Enantioselective Conjugate Addition Reactions via Iminium Activation 62 3.1 Introduction 62 3.1.1 Factors Influencing the Stereocontrol in Michael Additions Proceeding via Iminium Activation 64 3.2 Michael Reaction 66 3.2.1 a,ß-Unsaturated Aldehydes as Michael Acceptors 67 3.2.2 a,ß-Unsaturated Ketones as Michael Acceptors 80 3.3 Conjugate Friedel-Crafts Alkylation Reaction 87 3.4 Conjugate Hydrogen Transfer Reaction 91 3.5 Conjugate Addition of Heteroatom-based Nucleophiles 94 3.5.1 Oxa-Michael Reactions 94 3.5.2 Sulfa-Michael Reactions 97 3.5.3 Aza-Michael Reactions 99 3.5.4 Phospha-Michael Reactions 103 3.6 Concluding Remarks 106 References and Notes 106 Chapter 4 Enantioselective Conjugate Addition Reactions via Hydrogen-bonding Activation 112 4.1 Introduction 112 4.1.1 Some Relevant Aspects Influencing the Stereocontrol in Michael Additions Proceeding via Hydrogen-bonding Activation 116 4.2 Conjugate Addition of Stabilized Carbon Nucleophiles 119 4.2.1 Nitroalkenes as Michael Acceptors 120 4.2.2 Enones as Michael Acceptors 139 4.2.3 a,ß-Unsaturated Aldehydes as Michael Acceptors 146 4.2.4 Acrylic Acid Derivatives as Michael Acceptors 149 4.2.5 Other Michael Acceptors 152 4.3 Conjugate Friedel-Crafts Reactions 159 4.4 Conjugate Hydrogen-transfer Reactions 164 4.5 Conjugate Addition of Heteronucleophiles 167 4.5.1 Oxa-Michael Reactions 168 4.5.2 Sulfa-Michael Reactions 171 4.5.3 Aza-Michael Reactions 174 4.5.4 Phospha-Michael Reactions 177 4.6 Concluding Remarks 179 References and Notes 180 Contents ix Chapter 5 Enantioselective Conjugate Addition Reactions via Phase-transfer Catalysis 187 5.1 Introduction 187 5.1.1 Mechanistic Considerations Regarding Michael Additions Proceeding via Phase-transfer Catalysis 190 5.2 Conjugate Addition of Stabilized Carbon Nucleophiles 193 5.2.1 Enones as Michael Acceptors 193 5.2.2 Acrylic Acid Derivatives as Michael Acceptors 206 5.2.3 a,ß-Unsaturated Aldehydes as Michael Acceptors 212 5.2.4 Nitroalkenes as Michael Acceptors 214 5.2.5 Other Michael Acceptors 215 5.3 Conjugate Addition of Heteroatom-centered Nucleophiles 218 5.4 Concluding Remarks 219 References and Notes 219 Chapter 6 Enantioselective Conjugate Addition Reactions Proceeding via Other Types of Activation 222 6.1 Introduction 222 6.2 Enantioselective Conjugate Addition Reactions Catalyzed by N-heterocyclic Carbenes 223 6.2.1 The Intramolecular Enantioselective Stetter Reaction 225 6.2.2 The Intermolecular Enantioselective Stetter Reaction 230 6.3 Enantioselective Conjugate Addition Reactions Catalyzed by Chiral Bronsted Bases 233 6.3.1 Conjugate Addition of Carbon Nucleophiles 234 6.3.2 Conjugate Addition of Heteroatom-based Nucleophiles 236 6.4 Other Miscellaneous Enantioselective Conjugate Addition Reactions 238 6.5 Concluding Remarks 241 References and Notes 241 Chapter 7 Enantioselective Cascade Reactions Initiated by Conjugate Addition 244 7.1 Introduction 244 7.2 Cascade Processes Initiated by Conjugate Addition via Enamine Activation 245 7.2.1 Cascade Michael/AIdol Reactions 245 x Contents 7.2.2 Cascade Michael/Michael Reactions 248 7.2.3 Michael/Michael/Aldol Triple Cascade Reactions 250 7.2.4 Other One-pot Procedures Initiated by Michael Reactions Proceeding under Enamine Activation 254 7.3 Cascade Processes Initiated by Conjugate Addition via Iminium Activation 257 7.3.1 Michael/AIdol Cascade Reactions 257 7.3.2 Michael/Michael Cascade Reactions 266 7.3.3 Michael//oc-Alkylation Cascade Reactions 273 7.3.4 Other Cascades Initiated by Michael Reactions Using Stabilized Carbon Nucleophiles 276 7.3.5 Cascades Initiated by Conjugate Friedel-Crafts Reaction 279 7.3.6 Cascades Initiated by Conjugate Hydrogen-transfer Reaction 283 7.3.7 Cascades Initiated by Hetero-Michael Reaction 287 7.4 Cascade Processes Initiated by Conjugate Addition via H-bonding Activation 299 7.4.1 Michael/Henry and Michael/Aza-Henry Cascade Reactions 300 7.4.2 Michael/Michael Cascade Reactions 302 7.4.3 Michael/a-Alkylation Cascade Reactions 304 7.4.4 Other Cascades Initiated by Michael Reactions Using Stabilized Carbon Nucleophiles 306 7.4.5 Cascade Processes Initiated by Hetero-Michael Reactions 308 7.5 Cascade Processes Initiated by Conjugate Addition via Phase-transfer Catalysis 311 7.5.1 Michael/Elimination Cascade Reactions 311 7.5.2 Other Cascades Initiated by Michael Reactions using Stabilized Carbon Nucleophiles 315 7.5.3 Cascade Processes Initiated by Hetero-Michael Reactions 316 7.6 Cascade Processes Initiated by Conjugate Addition via Other Mechanisms of Activation 318 7.6.1 Cascade Processes Initiated by A^-heterocyclic Carbene-mediated Conjugate Additions 318 7.6.2 Cascade Processes Initiated by Conjugate Additions Proceeding via Ylide Formation 319 7.6.3 Other Miscellaneous Cascade Processes 321 7.7 Concluding Remarks 322 References and Notes 323 Appendix: Catalysts Referred to in the Text 330 Subject Index 340
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series RSC catalysis series
series2 RSC catalysis series
spellingShingle Vicario, Jose L.
Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules
RSC catalysis series
Additionsreaktion (DE-588)4141380-5 gnd
subject_GND (DE-588)4141380-5
title Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules
title_auth Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules
title_exact_search Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules
title_full Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules ed. by Jose L. Vicario ...
title_fullStr Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules ed. by Jose L. Vicario ...
title_full_unstemmed Organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules ed. by Jose L. Vicario ...
title_short Organocatalytic enantioselective conjugate addition reactions
title_sort organocatalytic enantioselective conjugate addition reactions a powerful tool for the stereocontrolled synthesis of complex molecules
title_sub a powerful tool for the stereocontrolled synthesis of complex molecules
topic Additionsreaktion (DE-588)4141380-5 gnd
topic_facet Additionsreaktion
url http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=026116249&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
volume_link (DE-604)BV035969664
work_keys_str_mv AT vicariojosel organocatalyticenantioselectiveconjugateadditionreactionsapowerfultoolforthestereocontrolledsynthesisofcomplexmolecules