Description

Book Synopsis
This book provides a noteworthy compilation of the groundbreaking methods of stereoselective synthesis, belonging to the repertoire of every modern practitioner of synthetic organic chemistry. The general principles underlying these processes are highlighted as they form the basis for the rapid and continuing developments in the field. The work also features illustrative examples of drug and natural product syntheses, resulting in a rich source of stimulating ideas for the efficient use of asymmetric reactions in the construction of stereochemically complex structures.


From the contents:

"Macrocyclic stereocontrol
"Carbonyl addition reactions
"alpha-Functionalization of enolates
"Aldol and allylation reactions
"Chiral acetals
"Alkene hydroboration, reduction, and oxidation
"Additions to C=N bonds and synthesis of amino acids
"Conjugate additions
"Chiral carbanions
"Metal-catalyzed allylations
"Cyclopropanations and CH-insertion reactions
"Sigmatropic rearrangements
"Diels-Alder and hetero-Diels-Alder reactions
"[3+2]- and [2+2]-cycloaddition reactions


Trade Review
"The book provides a collection of classic methods for stereoselective synthesis that have been developed over the past two decades - methods that should be at the command of every modern practitioner of synthetic organic chemistry." (Booknews, 1 April 2011)



Table of Contents
MACROCYCLIC STEREOCONTROL
Introduction
Background
Conformational Control in Medium-Sized Rings
Asymmetric Synthesis with Medium-Sized Rings
Case Studies in Natural Products Total Synthesis
Macrocyclic Stereocontrol in Cyclic Peptides
Appendix: Macrocycle Formation
CARBONYL ADITION REACTIONS
Introduction
Non-Chelated 1,2-Asymmetric Induction and the Operation of Steric and Electronic Effects
1,2-Asymmetric Induction Predicated on Chelation Control
1,3-Asymmetric Induction from CBeta Stereogenic Centers
Asymmetric Induction by Remote Stereocenters (Beyond 1,3-Induction)
Catalytic Enantioselective Carbonyl Additions of Arganozinc Species
Enantioselective Ketone Reduction
Enzymatic Reduction of Ketones
Enantioselective Formation of Cyanohydrins
Enantioselective Alkyne Additions
Asymmetric Carbonyl-Ene Reactions
ALPHA-FUNCTIONALIZATIONS OF ENOLATES
Introduction
Diastereoselective Alpha-Alkylations of Chiral Enolates
Heteroatom-Substituted Enolates
Asymmetric Enolate Alkylations Using Chiral Auxiliaries
Enantioselective Enolate Alkylations
Alpha-Hydroxylations of Enolates
Alpha-Halogenations of Enolates
ALDOL REACTIONS
Introduction
Chiral Enolates Through the Use of Chiral Auxiliaries or Chiral Controller Groups
Substrate Control with Chiral Carbonyl Compounds
Catalytic Enantioselective Aldol Reactions
ALLYLATIONS OF C=O BONDS
Introduction
Reactivity of Allylmetal Reagents
Boronate Additions
Enantioselective Additions of Optically Active Allylic Boron Reagents
Diastereoselecive Allylations with Chiral Boron Reagents
Mechanistic Aspects -
Lewis Acid-Promoted Addition of Allylsilanes and Allylstannanes to Aldehydes
Chelation Control in the Allylation of Alpha- and Beta-Alkoxy Aldehydes
Allylchromium Reagents
Diastereoselective Allylations with Chiral Silanes and Stannanes
Catalytic Asymmetric Allylations
CHIRAL ACETALS
Introduction
Diastereoselective Reactions of Chiral Acetals
Glycosylations
Spiroketals in Natural Product Synthesis
ALKENE HYDROBORATION
Introduction
Hydroborations with Acyclic Stereocontrol
Metal-Catalyzed Hydroborations
Asymmetric Hydroborations with Chiral Boranes
Catalytic Asymmetric Hydroboration, Hydrosilylation, and Hydroalumination
REDUCTIONS OF OLEFINS
Introduction
Diastereoselective Olefin Reductions by Catalytic Hydrogenation
Alternative Methods for Diastereoselective Olefin Reductions
Catalytic Asymmetric Olefin Hydrogenations
OXIDATIONS OF OLEFINS
Introduction
Diastereoselective Epoxidations
Enantioselective Epoxidations
Asymmetric Ring-Opening of Epoxides
Synthesis of Aziridines
Iodolactonizations and Other Olefin Cyclizations Induced by Electrophiles
Diastereoselective Dihydroxylations of Olefins
Enantioselective Dihydroxylations of Olefins
Enantioselective Aminohydroxylation of Olefins
AMINO ACIDS
Introduction
Enantioselective Hydrogenations of Alpha, Beta-Didehydroamino Acids
Enolate Alkylations in the Presence of Chiral Auxiliaries
Alkylation of Glycine Anion Equivalents in the Presence of Chiral Phase-Transfer Catalysts
Enolate Aminations
Enzymatic Syntheses of Alpha-Amino Acids
Catalytic Asymmetric Strecker Reactions
ADDITIONS TO C=N BONDS
Introduction
Substrate-Controlled Diastereoselective Additions to C=N Bonds
Additions to Imine Derivatives Bearing N-Bound Auxiliaries
Formation of Beta-Lactams Through Staudinger Reactions
Intramolecular Diastereoselective Iminium Ion Cyclizations
Pictet-Spengler Reactions
Catalytic Asymmetric Reductions of Imines and Imine Derivatives
Catalytic Enantioselective Mannich and Mannich-Type Reactions
Enantioselective Additions of Carbon Nucleophiles to C=N Bonds
CONJUGATE ADDITIONS
Introduction
Diastereoselective Conjugate Additions

Diastereoselective Conjugate Additions with Use of Chiral Auxiliaries
Enantioselective Conjugate Additions of Enolates and other Stabilized Carbon Nucleophiles
Enantioselective Conjugate Additions of Organometallic Species
Enantioselective Conjugate Additions of Radicals
Enantioselective Conjugate Additions of Heteroatom Nucleophiles
Conjugate Reductions
Catalytic Enantioselective Stetter Reactions
CHIRAL CARBONIONS
Introduction
Organolithium Reagents by Transmetalation of Organostannanes
Carbanions by Reductive Methods
Chiral Carbanions by Deprotonation
Sulfoxide- and Phosphorus-Stabilized Carbanions
Metal-Mediated Enantioselective Olefin Functionalizations
METAL-CATALYZED ALLYLATIONS
Introduction
Diastereoselective Palladium-Catalyzed Allylation Reactions
Enantioselective Palladium-Catalyzed Allylation Reactions
Iridium-Catalyzed Enantioselective Allylation Reactions
Copper-Catalyzed SN2' Allylation Reactions
Enantioselective Allylation Reactions Catalyzed by Other Transition Metals
Asymmetric Ring-Opening Reactions of Unsaturated Heterocycles
CYCLOPROPANATIONS AND C-H INSERTION REACTIONS
Introduction
Diastereoselective Cyclopropanations with Carbenoids Generated from Diazoalkanes
Enantioselective Dyclopropanations with Carbenoids Generated from Diazoalkanes
Diastereoselective Simmons-Smith Cyclopropanations
Enantioselective Simmons-Smith Cyclopropanations
Alternative Classes Cyclopropanations
Diastereoselective C-H Bonds
SIGMATROPIC REARRANGEMENTS
Introduction
Claisen and Claisen-Type [3,3]-Sigmatropic Rearrangements
Cope and Cope-Type [3,3]-Sigmatropic Rearrangements
[2,3]-Sigmatropic Rearrangements
Ene Reactions
Nazarov Cyclizations
DIELS-ALDER AND HETERO-DIELS-ALDER REACTIONS
Introduction
Diastereoselective Intermolecular Diels-Alder Reactions
Diastereoselective Intramolecular Diels-Alder Reactions
Diastereoselective Diels-Alder Reactions Using Chiral Auxiliaries
Catalytic Enantioselective Diels-Alder Reactions
Diastereoselective Hetero-Diels-Alder Reactions
Enantioselective Hetero-Diels-Alder Reactions
[3+2]- AND [2+2]-CYCLOADDITION REACTIONS
Introduction
Substrate-Controlled Diastereoselective [1,3]-Dipolar Cycloadditions
Diastereoselective [1,3]-Dipolar Cycloadditions Using Chiral Auxiliaries
Catalytic Enantioselective [1,3]-Dipolar Cycloadditions
[3+2]-Cycloadditions with Trimethylenemethane Equivalents
Ketene Cycloadditions
Photochemical [2+2]-Cycloadditions

Classics in Stereoselective Synthesis

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    A Hardback by Erick M. Carreira, Lisbet Kvaerno

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      View other formats and editions of Classics in Stereoselective Synthesis by Erick M. Carreira

      Publisher: Wiley-VCH Verlag GmbH
      Publication Date: 17/12/2008
      ISBN13: 9783527324521, 978-3527324521
      ISBN10: 3527324526

      Description

      Book Synopsis
      This book provides a noteworthy compilation of the groundbreaking methods of stereoselective synthesis, belonging to the repertoire of every modern practitioner of synthetic organic chemistry. The general principles underlying these processes are highlighted as they form the basis for the rapid and continuing developments in the field. The work also features illustrative examples of drug and natural product syntheses, resulting in a rich source of stimulating ideas for the efficient use of asymmetric reactions in the construction of stereochemically complex structures.


      From the contents:

      "Macrocyclic stereocontrol
      "Carbonyl addition reactions
      "alpha-Functionalization of enolates
      "Aldol and allylation reactions
      "Chiral acetals
      "Alkene hydroboration, reduction, and oxidation
      "Additions to C=N bonds and synthesis of amino acids
      "Conjugate additions
      "Chiral carbanions
      "Metal-catalyzed allylations
      "Cyclopropanations and CH-insertion reactions
      "Sigmatropic rearrangements
      "Diels-Alder and hetero-Diels-Alder reactions
      "[3+2]- and [2+2]-cycloaddition reactions


      Trade Review
      "The book provides a collection of classic methods for stereoselective synthesis that have been developed over the past two decades - methods that should be at the command of every modern practitioner of synthetic organic chemistry." (Booknews, 1 April 2011)



      Table of Contents
      MACROCYCLIC STEREOCONTROL
      Introduction
      Background
      Conformational Control in Medium-Sized Rings
      Asymmetric Synthesis with Medium-Sized Rings
      Case Studies in Natural Products Total Synthesis
      Macrocyclic Stereocontrol in Cyclic Peptides
      Appendix: Macrocycle Formation
      CARBONYL ADITION REACTIONS
      Introduction
      Non-Chelated 1,2-Asymmetric Induction and the Operation of Steric and Electronic Effects
      1,2-Asymmetric Induction Predicated on Chelation Control
      1,3-Asymmetric Induction from CBeta Stereogenic Centers
      Asymmetric Induction by Remote Stereocenters (Beyond 1,3-Induction)
      Catalytic Enantioselective Carbonyl Additions of Arganozinc Species
      Enantioselective Ketone Reduction
      Enzymatic Reduction of Ketones
      Enantioselective Formation of Cyanohydrins
      Enantioselective Alkyne Additions
      Asymmetric Carbonyl-Ene Reactions
      ALPHA-FUNCTIONALIZATIONS OF ENOLATES
      Introduction
      Diastereoselective Alpha-Alkylations of Chiral Enolates
      Heteroatom-Substituted Enolates
      Asymmetric Enolate Alkylations Using Chiral Auxiliaries
      Enantioselective Enolate Alkylations
      Alpha-Hydroxylations of Enolates
      Alpha-Halogenations of Enolates
      ALDOL REACTIONS
      Introduction
      Chiral Enolates Through the Use of Chiral Auxiliaries or Chiral Controller Groups
      Substrate Control with Chiral Carbonyl Compounds
      Catalytic Enantioselective Aldol Reactions
      ALLYLATIONS OF C=O BONDS
      Introduction
      Reactivity of Allylmetal Reagents
      Boronate Additions
      Enantioselective Additions of Optically Active Allylic Boron Reagents
      Diastereoselecive Allylations with Chiral Boron Reagents
      Mechanistic Aspects -
      Lewis Acid-Promoted Addition of Allylsilanes and Allylstannanes to Aldehydes
      Chelation Control in the Allylation of Alpha- and Beta-Alkoxy Aldehydes
      Allylchromium Reagents
      Diastereoselective Allylations with Chiral Silanes and Stannanes
      Catalytic Asymmetric Allylations
      CHIRAL ACETALS
      Introduction
      Diastereoselective Reactions of Chiral Acetals
      Glycosylations
      Spiroketals in Natural Product Synthesis
      ALKENE HYDROBORATION
      Introduction
      Hydroborations with Acyclic Stereocontrol
      Metal-Catalyzed Hydroborations
      Asymmetric Hydroborations with Chiral Boranes
      Catalytic Asymmetric Hydroboration, Hydrosilylation, and Hydroalumination
      REDUCTIONS OF OLEFINS
      Introduction
      Diastereoselective Olefin Reductions by Catalytic Hydrogenation
      Alternative Methods for Diastereoselective Olefin Reductions
      Catalytic Asymmetric Olefin Hydrogenations
      OXIDATIONS OF OLEFINS
      Introduction
      Diastereoselective Epoxidations
      Enantioselective Epoxidations
      Asymmetric Ring-Opening of Epoxides
      Synthesis of Aziridines
      Iodolactonizations and Other Olefin Cyclizations Induced by Electrophiles
      Diastereoselective Dihydroxylations of Olefins
      Enantioselective Dihydroxylations of Olefins
      Enantioselective Aminohydroxylation of Olefins
      AMINO ACIDS
      Introduction
      Enantioselective Hydrogenations of Alpha, Beta-Didehydroamino Acids
      Enolate Alkylations in the Presence of Chiral Auxiliaries
      Alkylation of Glycine Anion Equivalents in the Presence of Chiral Phase-Transfer Catalysts
      Enolate Aminations
      Enzymatic Syntheses of Alpha-Amino Acids
      Catalytic Asymmetric Strecker Reactions
      ADDITIONS TO C=N BONDS
      Introduction
      Substrate-Controlled Diastereoselective Additions to C=N Bonds
      Additions to Imine Derivatives Bearing N-Bound Auxiliaries
      Formation of Beta-Lactams Through Staudinger Reactions
      Intramolecular Diastereoselective Iminium Ion Cyclizations
      Pictet-Spengler Reactions
      Catalytic Asymmetric Reductions of Imines and Imine Derivatives
      Catalytic Enantioselective Mannich and Mannich-Type Reactions
      Enantioselective Additions of Carbon Nucleophiles to C=N Bonds
      CONJUGATE ADDITIONS
      Introduction
      Diastereoselective Conjugate Additions

      Diastereoselective Conjugate Additions with Use of Chiral Auxiliaries
      Enantioselective Conjugate Additions of Enolates and other Stabilized Carbon Nucleophiles
      Enantioselective Conjugate Additions of Organometallic Species
      Enantioselective Conjugate Additions of Radicals
      Enantioselective Conjugate Additions of Heteroatom Nucleophiles
      Conjugate Reductions
      Catalytic Enantioselective Stetter Reactions
      CHIRAL CARBONIONS
      Introduction
      Organolithium Reagents by Transmetalation of Organostannanes
      Carbanions by Reductive Methods
      Chiral Carbanions by Deprotonation
      Sulfoxide- and Phosphorus-Stabilized Carbanions
      Metal-Mediated Enantioselective Olefin Functionalizations
      METAL-CATALYZED ALLYLATIONS
      Introduction
      Diastereoselective Palladium-Catalyzed Allylation Reactions
      Enantioselective Palladium-Catalyzed Allylation Reactions
      Iridium-Catalyzed Enantioselective Allylation Reactions
      Copper-Catalyzed SN2' Allylation Reactions
      Enantioselective Allylation Reactions Catalyzed by Other Transition Metals
      Asymmetric Ring-Opening Reactions of Unsaturated Heterocycles
      CYCLOPROPANATIONS AND C-H INSERTION REACTIONS
      Introduction
      Diastereoselective Cyclopropanations with Carbenoids Generated from Diazoalkanes
      Enantioselective Dyclopropanations with Carbenoids Generated from Diazoalkanes
      Diastereoselective Simmons-Smith Cyclopropanations
      Enantioselective Simmons-Smith Cyclopropanations
      Alternative Classes Cyclopropanations
      Diastereoselective C-H Bonds
      SIGMATROPIC REARRANGEMENTS
      Introduction
      Claisen and Claisen-Type [3,3]-Sigmatropic Rearrangements
      Cope and Cope-Type [3,3]-Sigmatropic Rearrangements
      [2,3]-Sigmatropic Rearrangements
      Ene Reactions
      Nazarov Cyclizations
      DIELS-ALDER AND HETERO-DIELS-ALDER REACTIONS
      Introduction
      Diastereoselective Intermolecular Diels-Alder Reactions
      Diastereoselective Intramolecular Diels-Alder Reactions
      Diastereoselective Diels-Alder Reactions Using Chiral Auxiliaries
      Catalytic Enantioselective Diels-Alder Reactions
      Diastereoselective Hetero-Diels-Alder Reactions
      Enantioselective Hetero-Diels-Alder Reactions
      [3+2]- AND [2+2]-CYCLOADDITION REACTIONS
      Introduction
      Substrate-Controlled Diastereoselective [1,3]-Dipolar Cycloadditions
      Diastereoselective [1,3]-Dipolar Cycloadditions Using Chiral Auxiliaries
      Catalytic Enantioselective [1,3]-Dipolar Cycloadditions
      [3+2]-Cycloadditions with Trimethylenemethane Equivalents
      Ketene Cycloadditions
      Photochemical [2+2]-Cycloadditions

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