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Synthesis 2022; 54(21): 4764-4772
DOI: 10.1055/a-1683-9455
DOI: 10.1055/a-1683-9455
special topic
Asymmetric C–H Functionalization
Cationic Iridium/Chiral Bidentate Phosphoramidite Catalyzed Asymmetric Hydroarylation
Abstract
In this personal account, we summarize our investigations on the asymmetric direct addition of C(sp2)–H bonds to unsaturated bonds, such as C=O and C=C, using cationic iridium/chiral O-linked bidentate phosphoramidite (Me-BIPAM) and S-linked bidentate phosphoramidite (S-Me-BIPAM) catalyst systems.
1 Introduction
2 Highly Enantioselective Intramolecular Hydroarylation of α-Keto Amides
3 Highly Enantioselective Intermolecular Hydroarylation of Bicycloalkenes
4 Conclusion
Key words
asymmetric synthesis - C–H functionalization - hydroarylation - iridium catalysts - chiral bidentate phosphoramiditesPublication History
Received: 05 October 2021
Accepted after revision: 01 November 2021
Accepted Manuscript online:
01 November 2021
Article published online:
14 December 2021
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For transition-metal/BIPAM-catalyzed asymmetric hydroarylation of C=O and C=N with arylboronic acids, see:
For hydrogenation, see:
For the synthesis of linked BINOL, see:
For asymmetric hydroheteroarylation of alkenes, see:
For asymmetric intermolecular hydroarylations, see:
For asymmetric intramolecular hydroarylations, see:
For asymmetric intermolecular hydroarylations of 2-norbornene, see:
Conversion of amides: