An Improved Synthesis of 1,2,3,4-Tetrahydroisoquinolines via Intramolecular Cyclization of N-Acyl-N-(aryl)methyl-2-(phenylsulfinyl)ethylamine by Pummerer Reaction.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/45/5/45_5_813/_pdf
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Revisiting Classical Pummerer Cyclization Reaction: A Key Strategy for the Synthesis of (±)‐Quinagolide;ChemistrySelect;2022-07-25
2. Preventative effects of 1-methyl-1,2,3,4-tetrahydroisoquinoline derivatives (N-functional group loading) on MPTP-induced parkinsonism in mice;Canadian Journal of Physiology and Pharmacology;2022-07-01
3. Pummerer Synthesis of Chromanes Reveals a Competition between Cyclization and Reductive Chlorination;Organic Letters;2019-08-23
4. Transition-Metal-Free Oxidative Cross-Coupling of Triorganoindium Reagents with Tetrahydroisoquinolines;The Journal of Organic Chemistry;2019-07-11
5. Pummerer Cyclization Revisited: Unraveling of Acyl Oxonium Ion and Vinyl Sulfide Pathways;Organic Letters;2018-09-10
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