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Epoxides: Synthesis, Reactions and Uses
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Editors: Rick Reeves and Maryann Lawrence
Book Description:
This book opens with a discussion on the syntheses of acyclic polyketides by using epoxide opening reactions. The stereoselective epoxidations of allylic alcohols, including catalytic asymmetric epoxidation reactions and stereospecific reactions due to substrate-control, are described shortly. Afterwards, different epoxide opening reactions and applications in natural product synthesis are reviewed. The authors highlight the recent advances in catalytic one-pot synthesis of epoxides. The versatility of organometallic catalysts in epoxidation of alkenes are considered an important point of research in the context of these transformations. Later, occurrence of carotenoid 5,6-epoxides, their chemical synthesis, the separation of stereoisomers, some transformations of 5,6-epoxy-carotenoids, and their biological processes are described. Following this, the methodologies for the deoxygenation of epoxides using oxo-molybdenum and oxo-rhenium complexes as efficient catalysts are described, allowing “a large community of readers, in particularly the community that works in catalysis, organic and organometallic chemistry, ready access to the novel methodologies developed.” (Nova)


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Table of Contents:
Preface

Chapter 1. Epoxide Opening Transformations in Syntheses of Acyclic Polyketides (pp. 1-56)
(Seijiro Hosokawa)

Chapter 2. Recent Advances in Catalytic Synthesis of Epoxides Mediated by Organometallic Catalysts (pp. 57-106)
(Yu Lin Hu)

Chapter 3. Carotenoid 5,6-Epoxides (pp. 107-142)
(József Deli, Ágnes Farkas, and Péter Molnár)

Chapter 4. Deoxygenation of Epoxides Catalyzed by Oxo-Complexes (pp. 143-176)
(Ana Cristina Fernandes)

Index (pp. 177)

Total Pages: 182

   Series:
      Chemistry Research and Applications
   Binding: Softcover
   Pub. Date: 2018 - 1st Quarter
   ISBN: 978-1-53612-960-1
   Status: AV
  
Status Code Description
AN Announcing
FM Formatting
PP Page Proofs
FP Final Production
EP Editorial Production
PR At Prepress
AP At Press
AV Available
  
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Epoxides: Synthesis, Reactions and Uses