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  • TITLE
  • DECLARATION
  • CERTIFICATE
  • ACKNOWLEDGEMENT
  • CONTENTS
  • Preface
  • ABBREVIATIONS
  • 1 A BRIEF REVIEW OF THE DIPOLAR CYCLOADDITION REACTIONS OF QUINONOID COMPOUNDS
  • 1.1. General Introduction
  • 1.2. Benzoquinones
  • 1.2.1. Diels-Alder reactions of o-quinones
  • 1.2.2. Dipolar cycloadditions of benzoquinones
  • 1.2.2.a. Reaction with diazomethane
  • 1.2.2.b. Reaction with azomethine ylide
  • 1.2.2.c. Reaction with mesoionics
  • 1.2.2.d. Reaction with nitrile oxides
  • 1.2.2.e. Reaction with zwitterionic species
  • 1.3. Isatins
  • 1.4. Quinoneimides
  • 1.4.1. Stability and synthesis
  • 1.4.2. Chemistry of quinoneimides
  • 1.4.2.a. Addition reactions of quinoneimides
  • 1.4.2.b. Cycloaddition reactions of quinoneimides
  • 1.5. Definition of the problem
  • 1.6. Theoretical considerations
  • Fig. 5: Sustmanns Classification
  • 1.6.1. Geometries and electronic structure of 1, 3-dipoles
  • a. Closed shell i, 3-dipoles or Zwitterions
  • b. l, 3-Dipoles with weak diradical character
  • c. 1, 3-Dipoles with moderate diradical character
  • d. 1, 3-Dipoles with strong, diradical character
  • 1.7. References
  • 2 FORMAL[3+2] AND[2+3] DIPOLAR CYCLOADDITION OFALLYLSILANES TO QUINONOID COMPOUNDS
  • 2.1. Introduction
  • 2.1.1. Allylsilane as dipoles
  • 2.1.2. Mechanistic aspects
  • 2.1.3. The present work
  • 2.2. Results and discussion
  • 2.2.1. Reaction of allylsilane with o-quinones
  • 2.2.2. Reaction of allylsilane with isatins and its derivatives
  • 2.2.3. Reaction of allylsilane with quinoneimides
  • p-Quinone diimides
  • Fig. 11: I3c NMR spectrum of 18a
  • Fig. 12: Single crystal X-ray structure of 18a
  • Fig. 14: I3c NMR spectrum of 19a
  • p-Quinone monoimides
  • o-Quinoneimides
  • 2.3. Experimental
  • 2.3.1. Preparation of quinoneimides
  • Preparation of 1, 4-benzoquinone ditoluenesulfonimide (5a)
  • Preparation of 2, 5-dimethyl-1, ddibenzenesulfonimide (5b)
  • Preparation of 1, 4-benzoquinonedibenrimide (5c)
  • Preparation of 4-methyl-l, 2-benzoquinonedibenzenesulfonimide (7a)
  • Experimental Procedures and Data for the Compounds Synthesized
  • 2.4. References
  • 3 DIPOLAR CYCLOADDION OF para QUINONES AND para QUINONEIMIDES WITH CARBONYL COMPOUNDS
  • 3. 1. Introduction
  • 3.1.1. Present study
  • 3.2. Results and discussion
  • 3.2.1. Reaction of carbonyl ylides with p-quinones
  • 3.2.2. Reaction of carbonyl ylides with p-quinoneimides
  • 3.3. Theoretical considerations
  • 3.4. Experimental
  • 3.5. References
  • Summary
  • List of Publications