An expeditious approach to 1-aminoisoquinolines via an unexpected reaction of 2-alkynylbenzaldoxime, carbodiimide, with bromine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 articles.
1. For selected examples, see:
2. Design and Synthesis of Novel Isoquinoline-3-nitriles as Orally Bioavailable Kv1.5 Antagonists for the Treatment of Atrial Fibrillation
3. A New 1,2-Dihydroisoquinoline from the Sponge Petrosia similis
4. Inhibitory Mechanism of Papaverine on Carbachol-Induced Contraction in Bovine Trachea
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1. Alkaline-Metal-Promoted Divergent Synthesis of 1-Aminoisoquinolines and Isoquinolines;The Journal of Organic Chemistry;2024-01-09
2. Advances and applications of 2-alkynylbenzaldoxime as a valuable synthetic framework for synthesizing N-heterocycles;Tetrahedron;2023-07
3. Metal‐Free Facile Synthesis of Multisubstituted 1‐Aminoisoquinoline Derivatives with Dual‐State Emissions;Chemistry – An Asian Journal;2020-04-21
4. Ten years of progress in the synthesis of six-membered N-heterocycles from alkynes and nitrogen sources;Tetrahedron;2020-01
5. Rhodium-catalyzed C–H activation/annulation of amidines with 4-diazoisochroman-3-imines toward isochromeno[3,4-c]isoquinolines;Organic & Biomolecular Chemistry;2019
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