and others such as HAT, which are beyond the familiar N‐radical species addition.
Scheme 3.47 Electrochemical intermolecular oxidative C(sp3)–H/N–H cross‐coupling.
Source: Modified from Wu et al. [61].
Although an array of notable achievements has already been advanced in the recent years, there still remain certain challenges/opportunities in this field: (i) The N–H sources are generally limited to azoles, sulfonamides, secondary amides, carbamates, and diaryl amines. Only few examples have been developed that make use of primary amines or secondary amines. Therefore, developing a versatile strategy with a broader amine scope is still highly desirable; (ii) the direct amination of C(sp3)–H has only been realized for the aliphatic ones on the activated sites such benzylic or α‐positions to a heteroatom, and the HAT‐facilitated amination is mostly limited to the functionalization at the remote δ‐H to a nitrogen substitution. The exploration of more versatile C(sp3)–H aminations is also very attractive; (iii) highly enantioselective aminations as well as site‐specific aminations on general aromatic rings are still rarely achieved in the simple radical‐involved processes, which needs further investigation.
In the near future, further efforts in this area may focus on the development of new catalysts or combined catalytic systems to broaden the amination generality, both in photo‐ and electrochemical protocols. Comprehensive mechanistic investigations are also necessary for the elucidation of the activation mode of the direct aminations, which can provide a better understanding of the reaction pathway and conversely inspire the design of more elegant reactions with a broader scope. Moreover, application of chiral catalysts to coordinate with the radical intermediates or directing groups installed on the substrates would potentially address the issue of enantioselectivity. Further disclosures are anticipated to make the direct amination strategy one of the most valuable approaches for C—N bond construction.
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