Metal‐Free, Hindered, Regioselective Access to Multifunctional Groups Diarylamines via S N Ar Substitution of P‐Nitroso Aromatic Methyl Ether by Arylamines

Abstract Multifunctional groups diarylamines, an innovative product, efficiently produced from arylamines and p‐nitrosoanisole derivatives by intermolecular S N Ar under weak acid conditions. This S N Ar proceeds under mild reaction conditions, and more significantly, the substrates involved do not necessarily require strong electron‐withdrawing groups. Moreover, this S N Ar is characterized by resistance to space crowding, tolerance to halogen and nitroso functional groups, and high regioselectivity. Mechanistic observations suggest that the S N Ar is the result of the transfer of the positive charge center of the protonated nitroso group to the p‐methoxy group..

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:30

Enthalten in:

Chemistry – A European Journal - 30(2024), 11

Beteiligte Personen:

Zou, Shuliang [VerfasserIn]
Zhang, Yazhou [VerfasserIn]
Wu, Qin [VerfasserIn]
Zhao, Tianming [VerfasserIn]
Li, Yutao [VerfasserIn]
Liu, Bing [VerfasserIn]
Ma, Xianguo [VerfasserIn]

Anmerkungen:

© 2024 Wiley‐VCH GmbH

Umfang:

6

doi:

10.1002/chem.202303421

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

WLY017372658