Solid-phase synthesis of isoquinolinones using Bischler–Napieralski cyclization
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
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4. Preparation and Diastereoselective Birch Reduction−Alkylation of Chiral 3,4-Dihydro-1(2H)-isoquinolinones. Enantiospecific Syntheses and Opioid Receptor Affinities of Several Hydro-2,3- dimethyl-1H-7,12a-methanobenzo[6,7]cycloocta[1,2-c]pyridine-9-ols
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1. A Three-Step Method for the Preparation of N-Substituted 3,4-Dihydroisoquinolin-1(2H)-ones and Heteroaryl-Fused 3,4-Dihydropyridin-2(1H)-ones from 2-Bromobenzoate Precursors;The Journal of Organic Chemistry;2023-01-27
2. Bischler‐Napieralski Cyclization: A Versatile Reaction towards Functional Aza‐PAHs and Their Conjugated Polymers †;Chinese Journal of Chemistry;2021-09-09
3. Bischler‐Napieralski reaction;Catalysis from A to Z;2020-04-19
4. Traceless Solid-Phase Organic Synthesis;Chemical Reviews;2019-11-20
5. One-Pot Synthesis of 2-Benzyl-3,4-dihydro-2H-isoquinolin-1-ones Catalyzed by CuCl2;Chinese Journal of Organic Chemistry;2019
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