Recent Application of Chiral Aryliodine Based on the 2-Iodo­resorcinol Core in Asymmetric Catalysis

In memory of Prof. Kilian Muñiz (1970–2020).

Abstract

Chiral iodoarenes have been steadily increasing in importance in recent years, especially in enantioselective synthesis and catalysis. Since the development of the concept of chiral iodine(I/III) catalysis, the use of various chiral aryliodine frameworks has been explored in this area. This short review gives an overview of the use of chiral hypervalent iodine(I/III) reagents based on the 2-iodoresorcinol core with two attached two lactic side chains bearing ester or amide groups for the catalytic enantioselective dearomatization of phenol compounds, asymmetric oxidation of alkenes, and enantioselective α-functionalization of carbonyl compounds highlighting the excellent reactivities in terms of yield and enantioselectivity.

1 Introduction

2 Enantioselective Dearomatization of Phenol Derivatives

3 Asymmetric Oxidation of Alkenes

4 Enantioselective α-Functionalization of Carbonyl Compounds

5 Conclusion and Outlook

Key words

chiral aryliodines - asymmetric catalysis - 2-iodoresorcinol - oxidation - enantioselective synthesis

Publication History

Received: 28 September 2020

Accepted after revision: 08 October 2020

Article published online:
12 November 2020

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