Effects of Chiral Ligands on the Asymmetric Carbonyl-Ene Reaction

Atefeh Bakhtiari; Javad Safaei-Ghomi

doi:10.1055/s-0037-1611875

Synlett, Table of Contents

Synlett 2019; 30(15): 1738-1764
DOI: 10.1055/s-0037-1611875

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Effects of Chiral Ligands on the Asymmetric Carbonyl-Ene Reaction

Atefeh Bakhtiari

,

Javad Safaei-Ghomi∗

Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan, P.O. Box 87317-51167, Iran Email: safaei@kashanu.ac.ir

› Author Affiliations

Abstract

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Abstract

The carbonyl-ene reaction is one of the most well-known reactions for C–C bond formation. Based on frontier molecular orbitals (FMO), carbonyl-ene reactions occur between the highest occupied molecular orbital (HOMO) of the ene compound bearing an active hydrogen atom at the allylic center and the lowest unoccupied molecular orbital (LUMO) of the electron-deficient enophile, which is a carbonyl compound. A high activation barrier enforces the concerted ene reaction rather than a Diels–Alder reaction at high temperature. Employing a catalytic system can eliminate defects in the ene reaction, and chiral catalysts promote the reaction under mild conditions to produce optically active compounds. In this account, we highlight investigations on the effects of various classes of chiral ligands on intermolecular and intramolecular carbonyl-ene reactions.

1 Introduction

2 Biaryl-Type Chiral Ligands

3 C ₁- and C ₂-Symmetric Bis(oxazoline) Ligands

4 Schiff Base Ligands

5 N,N′-Dioxide Ligands

6 Conclusions

Key words

carbonyl-ene reactions - biaryl ligands - bis(oxazoline) ligands - Schiff base ligands - salen ligands - N,N′-dioxide ligands

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References

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