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9781849731294

The Chemistry of the Morita-Baylis-Hillman Reaction

by ; ; ;
  • ISBN13:

    9781849731294

  • ISBN10:

    1849731292

  • Format: Hardcover
  • Copyright: 2011-04-04
  • Publisher: Royal Society of Chemistry

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Summary

Carbon-carbon bond formations and functional group transformations are the most fundamental reactions for the construction of molecular frameworks and are at the forefront of organic chemistry research. The Morita-Baylis-Hillman (MBH) type reactions possess the two most important requirements - atom economy and generation of multi-functional groups. The last decade has seen exponential growth of the MBH reaction and its applications. In fact, it is already one of the most powerful carbon-carbon bond-forming methods widely used in organic synthesis. Since the 1990s, more and more research groups have initiated work on different aspects of the MBH reaction. These have focused on the scope of the substrates, novel catalysts (especially chiral catalysts), reaction mechanisms, and synthetic applications. Consequently, there is now a need for a reference detailing the chemistry of this important reaction. This unique book summarizes the MBH reaction, aza-MBH reaction and asymmetric MBH/aza-MBH reaction including the latest research and mechanistic investigations. It provides a complete overview of MBH-type reactions aimed at synthetic organic chemists of all levels within academia and industry. The chapters cover the; origin and growth of the Morita-Baylis-Hillman reaction; reactant classes and reaction conditions; catalytic mechanisms; achiral and chiral catalytic systems; transformations of functional groups; use of Morita-Baylis-Hillman adducts and derivatives as starting materials to construct compounds with carbocyclic or heterocyclic frameworks, and the applications of the MBH reaction in synthesizing natural products.

Table of Contents

Morita-Baylis-Hillman Reactionp. 1
Introductionp. 1
Mechanism of Morita-Baylis-Hillman Reactionp. 2
Amine-catalyzed Mechanismp. 2
Phosphine-catalyzed Mechanismp. 5
Activated Olefinsp. 8
Acrylatesp. 9
Acrylonitrilesp. 12
Allenes, Acetylenes and Dienesp. 13
Acrylamidesp. 17
Acroleinp. 20
¿,ß-Unsatyurated Ketonesp. 20
ß-Substituted Activated Olefinsp. 24
Nitroalkenesp. 25
Vinyl Sulfones, Vinyl Sulfoxides and Vinyl Sulfonatesp. 26
Vinylphosphonatesp. 27
Miscellaneous Activated Olefinsp. 27
Electrophilesp. 28
Aldehydesp. 28
Ketonesp. 39
¿-Keto Esters, ß-Keto Lactones, ß-Keto Lactams and Diketones (ß-Keto Carbonyl Compounds)p. 41
Imines and Iminium Saltsp. 44
Other Electrophilesp. 48
Multicomponent One-pot Reactionp. 49
Intramolecular Morita-Baylis-Hillman Reactionp. 51
Ionic Liquid as Reaction Mediap. 61
Referencesp. 69
Catalytic Systems for the Morita-Baylis-Hillman Reactionp. 79
Introductionp. 79
Amine-catalyzed Systemp. 79
Achiral Aminep. 79
Chiral Aminep. 104
Cinchona-derived Catalystsp. 104
Unnatural Tertiary Aminesp. 116
Non-natural Tertiary Amine/Thiourea (Phenol) Catalystsp. 121
Phosphine-catalyzed Systemp. 122
Achiral Phosphinep. 122
Chiral Phosphinep. 132
TiCI4-Lewis Acid Mediated Catalyzed Systemp. 146
Chalcogenide-Lewis Acid Mediated Systemp. 155
Chalcogenide-TiCI4 Mediated Systemp. 156
Chalcogeni de-media ted System in the Presence of Other Lewis Acidsp. 163
Substrates Containing a Chalcogenide Groupp. 166
p. Co-catalyzed
Proline as Co-catalystp. 170
(Thio)ureas as Co-catalystp. 175
Other Reagents as Co-catalystsp. 180
Polymer-supported Catalysts for the Morita-Baylis-Hillman Reactionp. 192
Referencesp. 198
Transformations of Functional Groups in Morita-Baylis-Hillman Adductsp. 209
Introductionp. 209
Transformations of an Hydroxy! Groupp. 209
Esterification and Etherificationp. 209
Halogenationp. 216
Miscellaneous Transformationsp. 221
Friedel-Crafts Reactionp. 222
Isomerizationp. 227
Heck Reactionp. 230
Hydrogenationp. 233
Diels-Alder Reactionp. 238
Nucleophilic Additionp. 242
Carbon Nucleophilesp. 242
Nitrogen Nucleophilesp. 260
Oxygen Nucleophilesp. 270
Sulfur Nucleophilesp. 274
Phosphorus Nucleophilesp. 278
Other Nucleophilesp. 280
Radical Reactionsp. 284
Metathesis Reactionp. 290
Other Transformationsp. 295
Epoxidation and Aziridination Reactionsp. 295
Michael Addition Reactionsp. 299
Miscellaneousp. 305
Conclusionsp. 311
Referencesp. 311
Morita-Baylis-Hillman Adducts or Derivatives for the Construction of Cyclic Frameworksp. 325
Introductionp. 325
Synthesis of Cyclic Hydrocarbon Compoundsp. 326
Cyclopropane Ring Systemsp. 326
Five-membered-ring Carbocyclic Compoundsp. 327
Six-membered-ring Carbocyclic Compoundsp. 332
Aromatic Compoundsp. 338
Bridged Compoundsp. 344
Medium-sized-ring Carbocyclic Compoundsp. 350
Synthesis of Oxygen-containing Heterocyclic Compoundsp. 353
Oxiranesp. 353
b-Lactonesp. 356
s-Butyrolactonesp. 356
Furan-ring Derivativesp. 362
Pyransp. 368
Pyran-2-onesp. 370
Coumarin Derivativesp. 376
Medium-sized-ring Oxygen-containing Heterocyclesp. 379
Synthesis of Nitrogen-containing Heterocyclic Compoundsp. 382
Aziridinesp. 382
Azetidinesp. 383
b-Lactamsp. 384
Pyrrole Derivativesp. 389
Indoles and Indolizinesp. 404
Piperidines and Pyridinesp. 408
Quinolinesp. 414
Medium-sized-ring Nitrogen-containing Heterocyclesp. 428
Construction of Nitrogen Heterocycles Containing Two Nitrogen Atomsp. 438
Polyheterocyclic Compounds Containing a Nitrogen Atomp. 441
Synthesis of Other Heterocyclic Compoundsp. 452
Referencesp. 461
Application of Morita-Baylis-Hillman Reaction for the Synthesis of Natural Productsp. 485
Introductionp. 485
Acaterinp. 485
Analogues of N-Benzoyl-syn-phenylisoserine, (S)-ß-Homoserine and (S)Aspartic Acidp. 486
Asmarines A and Bp. 487
Aza Analogues of the Tricyclic Skeleton of Daphnane and the ABC Ring System of Phorbolp. 489
N-Boc-dolaproinep. 492
Borrelidinp. 492
(2E)-2-Butyloct-2-enalp. 493
Caribenolide Ip. 494
Clusianone and Polycyclic Polyprenylated Acylphloroglucinols (PPAPs)p. 494
Cyclic Peptidesp. 497
(-)-(Z)-Deoxypukalidep. 497
Diversonolp. 499
Dolichol Analoguesp. 503
Dykellic Acid and Gelastatin Analoguesp. 503
(+)-Efaroxanp. 505
Epopromycin Bp. 505
Eupomatilone 2p. 505
Fleursandol®p. 511
(+)-Frondosin Ap. 514
Furaquinocinsp. 515
(+)-Heliotridine and (-)-Retronecinep. 517
Luminacin Dp. 519
Mycestericin Ep. 519
Oxyisoterihaninep. 521
Phaseolinic Acidp. 521
Pinnatoxin Ap. 523
Salinosporamide A and its Analoguesp. 523
Selenomilfasartanp. 525
Solanoeclepin Ap. 525
Sordarin Corep. 527
(-)-Spinosyn Ap. 530
(-)-Spirotryprostatin Bp. 530
Syributins and Syringolides, Spyhydrofurans and Secosyrinsp. 532
Tacamoninep. 532
Core of Eleutherobinp. 538
Trioxacarcinosides Bp. 538
Tubelactomicinp. 540
6-Tuliposide Bp. 542
(R)-Umbelactonep. 543
Referencesp. 543
Subject Indexp. 552
Table of Contents provided by Ingram. All Rights Reserved.

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