Asymmetric Synthesis V2

1st Edition - December 1, 1983
Imprint: Academic Press
Editor: James Morrison
Language: English
Paperback ISBN:
9 7 8 - 0 - 1 2 - 4 3 3 4 2 4 - 3
eBook ISBN:
9 7 8 - 0 - 3 2 3 - 1 5 7 3 6 - 0

Asymmetrie Synthesis, Volume 2: Stereodifferentiating Addition Reactions, Part A is concerned with asymmetric addition reactions. This volume contains chapters that cover B-H… Read more

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Asymmetrie Synthesis, Volume 2: Stereodifferentiating Addition Reactions, Part A is concerned with asymmetric addition reactions. This volume contains chapters that cover B-H additions across carbon-carbon and carbon-oxygen double bonds; carbonyl reductions using chiral modifications of lithium aluminum hydride and chiral dihydropyridines; additions of achiral and chiral nucleophiles to chiral and achiral aldehydes and ketones; organometal additions to chiral vinylic sulfoxides; and description of imine and enamine alkylations. Chemists will find the book interesting.

Contributors

Preface

1. Asymmetric Hydroboration

I. Introduction

II. Diisopinocampheylborane

III. Dilongifolylborane

IV. Limonylborane

V. Monoisopinocampheylborane

VI. Conclusion

References

2. Reductions with Chiral Boron Reagents

I. Introduction

II. Chirally Modified Boranes

III. Chirally Modified Borohydrides

References

3. Reductions with Chiral Modifications of Lithium Aluminum Hydride

I. Introduction

II. Alcohol-Modified Lithium Aluminum Hydride

III. Amine-Modified Lithium Aluminum Hydride

IV. Amino Alcohol-Modified Lithium Aluminum Hydride

V. Aminodiol-Modified Lithium Aluminum Hydride

VI. Conclusions

References

4. Reductions with Chiral Dihydropyridine Reagents

I. Introduction

II. Summary of the Mechanistic Studies of NADH Model Reactions

III. Asymmetric Reductions with Chiral NADH Model Compounds

IV. Factors Affecting Product Stereochemistry in Asymmetric Reductions with Chiral NADH Model Compounds

V. Approach to Chiral NADH Models of Higher Stereoselectivity

VI. Simulation of Enzyme Active Site Composed of Peptide Chain

VII. Concluding Remarks

References

5. Application of Cram's Rule: Addition of Achiral Nucleophiles to Chiral Substrates

I. Introduction

II. Variation of Reaction Conditions

III. Application of Cram's Rule to Asymmetric Synthesis

IV. Remote Stereochemical Control

References

6. Addition of Chiral Nucleophiles to Aldehydes and Ketones

I. Introduction

II. Organometallic Reagents Used in a Chiral Environment

III. Addition of Carbanions a to a Chiral Sulfoxide Group

IV. Chiral Ester Enolates

References

7. Noncatalytic Additions to α,β-Unsaturated Carbonyl Compounds

I. Introduction

II. Conjugate Additions of Chiral α,β-Unsaturated Carbonyl Derivatives

III. Conjugate Additions with Chiral Nucleophiles

References

8. Addition of Organometallic Reagents to Chiral Vinylic Sulfoxides

I. Introduction

II. 1-Alkenyl Sulfoxides

III. 2-Alkenyl Sulfoxides

IV. 2-Cycloalkenone Sulfoxides

V. Conclusion

References

9. Alkylation of Imine and Enamine Salts

I. Introduction

II. Formation of Azaallyl Metal Reagents and Enamines

III. Structure of Azaallyl Metal Reagents

IV. Electrophilic Substitution of Azaallyl Metal Regents and Enamines

V. Asymmetric Syntheses Employing Chiral Azaallyl Metal Reagents

VI. Asymmetric Syntheses Employing Chiral Enamines

References

Index

Life Sciences

Physical Sciences & Engineering

Social Sciences & Humanities

Health

Asymmetric Synthesis V2

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