Brønsted Acid‐Catalyzed Asymmetric Ring‐Closing Alkylation of Inert N‐substituted Pyrroles with α, β‐Unsaturated Ketones-Reference-Cited by-同舟云学术

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Brønsted Acid‐Catalyzed Asymmetric Ring‐Closing Alkylation of Inert N‐substituted Pyrroles with α, β‐Unsaturated Ketones

Published:2019-07-03 Issue:16 Volume:361 Page:3694-3697
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Wei Zhao¹²,Zhang Jinlong¹,Yang Huameng¹,Jiang Gaoxi¹

Affiliation:

1. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Center for Excellence in Molecular Synthesis, Su-zhou Research Institute of LICP, Lanzhou Institute of Chemical Physics (LICP)Chinese Academy of Sciences Lan-zhou 730000 People's Republic of China

2. University of Chinese Academy of Sciences Beijing 100049 People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201900546

Reference43 articles.

1. For reviews see:

2. Pyrrole Syntheses by Multicomponent Coupling Reactions

3. Direct Coupling of Pyrroles with Carbonyl Compounds: Short Enantioselective Synthesis of (S)-Ketorolac

4. Total Synthesis of (−)-Rhazinilam: Asymmetric C−H Bond Activation via the Use of a Chiral Auxiliary

5. Chemistry and Biology of Roseophilin and the Prodigiosin Alkaloids: A Survey of the Last 2500 Years

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