Ring-opening reactions of N-aryl-,1,2,3,4-tetrahydroisoquinoline derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Reaction ofN-nitroaryl-1,2,3,4-tetrahydroisoquinoline derivatives with oxygen
2. Clegg, W; Creighton, J.R.; Hedley, K.A.; Raper, E.S.; Standorth, S.P. to be published.
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4. Beiträge zur Chemie der heterocyclischen pseudobasischen Aminocarbinole, XX. Herstellung von 3.4‐Dihydro‐isochinoliniumsalzen aus primären Aminen und 2‐[β‐Brom‐äthyl]‐benzaldehyd
5. Heterocyclic Pseudo Bases
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1. Difunctionalization of the C–N Bond through tert-Butylnitrite-Initiated C–N Cleavage of 1,2,3,4-Tetrahydroisoquinolines and N,N′-Diarylimidazolidines under Transition-Metal-Free Conditions;The Journal of Organic Chemistry;2019-09-09
2. Synthesis and biological evaluation of 1-amino isochromans from 2-bromoethyl benzaldehyde and amines in acid medium;Bioorganic & Medicinal Chemistry Letters;2018-01
3. Metal-Free C−C Bond Cleavage: One-Pot Access to 1,4-Benzoquinone-linked N -Formyl Amides/Sulfonamides/Carbamates using Oxone;Asian Journal of Organic Chemistry;2017-07-03
4. Mechanically activated ring-opening reactions of N-acyl-1,2,3,4-tetrahydroisoquinolines derived from the synthesis of praziquantel intermediate;Tetrahedron;2015-09
5. Electrophilic Halogenation of Arenes;Side Reactions in Organic Synthesis II;2014-05-30
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