A Very Mild Access to 3,4-Dihydroisoquinolines Using Triphenyl Phosphite-Bromine-Mediated Bischler-Napieralski-Type Cyclization-Reference-Cited by-同舟云学术

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A Very Mild Access to 3,4-Dihydroisoquinolines Using Triphenyl Phosphite-Bromine-Mediated Bischler-Napieralski-Type Cyclization

Published:2008-10-15 Issue:18 Volume:2008 Page:2807-2810
ISSN:0936-5214
Container-title:Synlett
language:en
Short-container-title:Synlett

Author:

Prati Fabio,Vaccari Daniele,Davoli Paolo,Ori Claudia,Spaggiari Alberto

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0028-1083544

Cited by 10 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. Chemo‐Enzymatic One‐Pot Two‐Step Functionalization of 1,2,3,4‐Tetrahydroisoquinolines by Monoamine Oxidase‐Ugi‐Joullié Reaction Sequence;European Journal of Organic Chemistry;2022-02-23

2. Bischler‐Napieralski Cyclization: A Versatile Reaction towards Functional Aza‐PAHs and Their Conjugated Polymers †;Chinese Journal of Chemistry;2021-09-09

3. Comprehensive Strategies for the Synthesis of Isoquinolines: Progress Since 2008;Advanced Synthesis & Catalysis;2020-09-02

4. Cp*Co(III)-Catalyzed γ-Selective C–H Allylation/Hydroamination Cascade for the Synthesis of Dihydroisoquinolines;Organic Letters;2019-12-03

5. 15.5.4 Isoquinolines (Update 2019);Knowledge Updates 2019/1;2019

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