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Synlett 2019; 30(13): 1525-1535
DOI: 10.1055/s-0037-1611861
DOI: 10.1055/s-0037-1611861
account
Electrophilic Amination: An Update
We thank the National Institute of General Medical Sciences (R01 GM-114609-04), the National Science Foundation (CAREER:SusChEM CHE-1546097) and the Robert A. Welch Foundation (Grant C-1764) for financial support. L.K. gratefully acknowledges the generous financial support of Rice University.Weitere Informationen
Publikationsverlauf
Received: 23. April 2019
Accepted after revision: 20. Mai 2019
Publikationsdatum:
08. Juli 2019 (online)
Abstract
In this account, we provide an overview of some recent advances in electrophilic amination methodologies that have been developed in the Kürti group over the last seven years. Our group’s focus has been to develop novel amination methodologies that directly yield N-unprotected amine products.
1 Introduction
2 Amination of Boronic Acids
3 Aziridination of Unactivated Olefins
4 Rhodium-Catalyzed C–H Amination of Arenes
5 Synthesis of Carbazoles
6 Amination of Aryl- and Alkylmetals
7 Doubly Electrophilic N-Linchpin Reagents
8 Aza-Rubottom Oxidation of Silyl Enol Ethers
9 Summary
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For C–N cross-coupling reviews, see:
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