(PhO)3P·Cl2-Promoted Bischler-Napieralski-Type Cyclization: a Mild Access to β-Carbolines
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2005-862394.pdf
Cited by 19 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
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3. Metal-free propargylation/aza-annulation approach to substituted β-carbolines and evaluation of their photophysical properties;Organic & Biomolecular Chemistry;2019
4. 10.23 Product Class 23: Pyrido[X,Y-b]indoles (Carbolines);Knowledge Updates 2018/2;2018
5. Computational study on the synthesis of 1-phenyl-3,4-dihydro-β-carboline: T3P®-promoted one-pot formation from tryptamine vs. POCl3-mediated ring closure of Nb-benzoyltryptamine. The first DFT investigation of the Bischler-Napieralski reaction;Computational and Theoretical Chemistry;2016-12
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