Cho, Seoyoung published the artcile1,2-Difunctionalization of Aryl Triflates: A Direct and Modular Access to Diversely Functionalized Anilines, Application In Synthesis of 5961-59-1, the main research area is aryl triflate amine iodine three component aminoiodination reaction; iodoaniline preparation; bomo methylaniline aryl triflate palladium catalyst arylation; methylcarbazole preparation.
Ortho-amino difunctionalization of aryl triflates was achieved via a three-component reaction. The cascade reaction proceeded through a zincate base-mediated deprotonative formation of a reactive aryne intermediate, in-situ nucleophilic addition, and coupling with electrophilic partners. This strategy leverages the advantageous reactivity of organozincate intermediates, enabling the installation of various functionalities such as amine, azide, oxygen, sulfur, halide, alkynyl, aryl, vinyl, and alkyl groups in a modular manner for the synthesis of diverse aniline skeletons.
Organic Letters published new progress about Amination. 5961-59-1 belongs to class isoquinoline, name is 4-Methoxy-N-methylaniline, and the molecular formula is C8H11NO, Application In Synthesis of 5961-59-1.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem