Development of Novel Hydrogen-Bond Donor Catalysts

  • Tsubasa¬†Inokuma

Part of the Springer Theses book series (Springer Theses)

Table of contents

  1. Front Matter
    Pages i-xiv
  2. Tsubasa Inokuma
    Pages 1-5
  3. Tsubasa Inokuma
    Pages 7-49
  4. Tsubasa Inokuma
    Pages 51-104
  5. Tsubasa Inokuma
    Pages 105-106
  6. Back Matter
    Pages 107-107

About this book


This work describes novel, effective hydrogen-bond (HB) donor catalysts based on a known bifunctional tertiary amine-thiourea, a privileged structure, which has been proven to be one of the most widely used organocatalysts. These HB donor catalysts derived from quinazoline and benzothiadiazine were initially synthesized as novel HB donors with their HB-donating abilities being measured by analytical methods. They were found to be effective for a variety of asymmetric transformations including Michael reactions of a, b-unsaturated imides and hydrazination reactions of 1,3-dicarbonyl compounds. Thiourea catalysts that have an additional functional group are also described. Specifically, thioureas that bear a hydroxyl group were synthesized and subsequently used as novel bifunctional organocatalysts for catalytic, asymmetric Petasis-type reactions involving organoboronic acids as nucleophiles. These addition reactions were difficult to achieve using existing organocatalysts. One of the developed catalytic methods can be applied to the synthesis of biologically interesting peptide-derived compounds possessing unnatural vinyl glycine moieties. These findings introduce new criteria required for the development of organocatalysts for asymmetric reactions, thus making a significant contribution to the field of organocatalysis.


Asymmetric Organocatalyst Bifunctional Thiourea HB Donor Catalysts Hydrazination Hydrogen Bond Michael Reaction Organoboronic Acid Petasis Reaction

Authors and affiliations

  • Tsubasa¬†Inokuma
    • 1
  1. 1.The Scripps Research InstituteLa JollaUSA

Bibliographic information