Produktbild: Linker Strategies in Solid-Phase Organic Synthesis

Linker Strategies in Solid-Phase Organic Synthesis

Fr. 288.00

inkl. gesetzl. MwSt., Versandkostenfrei


Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

01.12.2009

Herausgeber

Peter Scott

Verlag

John Wiley & Sons Inc

Seitenzahl

706

Maße (L/B/H)

25.3/19.9/4.3 cm

Gewicht

1498 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-0-470-51116-9

Beschreibung

Rezension

"It is without a doubt an invaluable addition to any university or corporate library serving organic and biochemical researchers." (CHOICE, September 2010)
"This book is a useful complement to literature reviews as well as other SPOS books. It will be a valuable resource for university libraries and an excellent first source for practitioners of solid-phase organic synthesis." (JACS, 2010)

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

01.12.2009

Herausgeber

Peter Scott

Verlag

John Wiley & Sons Inc

Seitenzahl

706

Maße (L/B/H)

25.3/19.9/4.3 cm

Gewicht

1498 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-0-470-51116-9

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

Noch keine Bewertungen vorhanden

Verfassen Sie die erste Bewertung zu diesem Artikel

Helfen Sie anderen Kundinnen und Kunden durch Ihre Meinung.

Kundinnen und Kunden meinen

Bewertungen (0)

  • Produktbild: Linker Strategies in Solid-Phase Organic Synthesis
  • Foreword.
     
    Preface.
     
    List of Contributors.
     
    About the Editor.
     
    Abbreviations.

    I: INTRODUCTION.

    Chapter 1: General Introduction (Scott L. Dax).
     
    1.1 Introduction, Background and Pivotal Discoveries.
     
    1.2 Fundamentals of Conducting Solid-Phase Organic Chemistry.
     
    1.3 Concluding Comments.
     
    1.4 Personal Perspective and Testimony: Solid-phase Mannich Chemistry.
     
    1.5 References.

    II: TRADITIONAL LINKER UNITS FOR SOLID-PHASE ORGANIC SYNTHESIS.

    Chapter 2: Electrophile Cleavable Linker Units (Michio Kuruso).
     
    2.1 Introduction.
     
    2.2 Resins for use with Electrophilic Linkers.
     
    2.3 Electrophile Cleavable Linkers.
     
    2.4 Conclusion.
     
    References.

    Chapter 3: Nucleophile Cleavable Linker Units (Andrea Porcheddu and Giampaolo Giacomelli).
     
    3.1 Introduction.
     
    3.2 Linker Units.
     
    3.3 Nucleophilic Labile Linker Units.
     
    3.4 Conclusion.
     
    References.

    Chapter 4: Cyclative Cleavage as a Solid-Phase Strategy (A. Ganesan).
     
    4.1 Introduction.
     
    4.2 C-N bond formation.
     
    4.3 C-O bond formation.
     
    4.4 C-C bond formation.
     
    4.5 Conclusion.
     
    References.

    Chapter 5: Photolabile Linker Units (Christian Bochet and Sébastien Mercier).
     
    5.1 Introduction.
     
    5.2 Linkers Based on the Ortho-Nitrobenzyloxy Function.
     
    5.3 Linkers Based on the Ortho-Nitrobenzylamino Function.
     
    5.4 Linkers Based on the ±-Substituted Ortho-Nitrobenzyl Group.
     
    5.5 Linkers Based on the Ortho-Nitroveratryl Group.
     
    5.6 Linkers Based on the Phenacyl Group.
     
    5.7 Linkers Based on the Para-Methoxyphenacyl Group.
     
    5.8 Linkers Based on the Benzoin Group.
     
    5.9 Linkers Based on the Pivaloyl Group.
     
    5.10 Traceless Linkers.
     
    5.11 Other Types of Photolabile Linker Units.
     
    5.12 Conclusion.
     
    References.

    Chapter 6: Safety-Catch Linker Units (Sylvain Lebreton and Marcel Pátek).
     
    6.1 Introduction.
     
    6.2 Activation of a carbonyl group by the inductive effect (I-) of an adjacent substituent.
     
    6.3 Activation by the mesomeric effect (M-) of the X-Y=Z moiety adjacent to a carbonyl group.
     
    6.4 Activation by the positive mesomeric effect (M+) of the -X-Y=Z moiety adjacent to a N-acyl or O-alkyl group.
     
    6.5 Aromatic SNAr substitution.
     
    6.6 Fragmentation by 2-elimination.
     
    6.7 Safety-catch linker for release in aqueous buffers.
     
    6.8 Photochemical activation.
     
    6.9 Miscellaneous safety-catch linkers.
     
    6.10 Conclusion.
     
    6.11 References.

    Chapter 7: Enzyme Cleavable Linker Units (Mallesham Bejugam and Sabine L. Flitsch).
     
    7.1 Introduction.
     
    7.2 Enzyme Cleavable Linker Units.
     
    7.3 Conclusion.
     
    References.

    III: MULTIFUNCTIONAL LINKER UNITS FOR DIVERSITY-ORIENTED SYNTHESIS.

    Chapter 8: An Introduction to Diversity-Oriented Synthesis (Richard J. Spandl, Gemma L. Thomas, Monica Diaz-Gavilan, Kieron M. G. O'Connell and David R. Spring).
     
    8.1 Introduction.
     
    8.2 Exploring Chemical Space.
     
    8.3 Sources of Skeletally Diverse Small Molecules.
     
    8.4 Enriching Chemical Space Using DOS.
     
    8.5 The Subjective Nature of 'Diversity'.
     
    8.6 Differing Strategies Towards Similar Goals.
     
    8.7 Generating Skeletal Diversity.
     
    8.8 DOS and Solid-Phase Organic Synthesis.
     
    8.9 Conclusion.
     
    References.

    Chapter 9: T1 and T2 -