Rapid Generation of Tetrahydropyridines and Tetrahydroquinolines by Dearomative Cyanation/Grignard Addition-Reference-Cited by-同舟云学术

Rapid Generation of Tetrahydropyridines and Tetrahydroquinolines by Dearomative Cyanation/Grignard Addition

Published:2022-04-14 Issue:10 Volume:17 Page:
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chemistry An Asian Journal

Author:

Zheng Shixin¹,Wang Dong²^ORCID,Huang Mindong¹,Yu Peng¹

Affiliation:

1. College of Biotechnology Tianjin University of Science and Technology Tianjin 300457 P. R. China

2. State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources College of Chemistry Xinjiang University Urumqi 830017 Xinjiang P. R. China

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.202200077

Reference63 articles.

1. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

3. Advances in the Chemistry of Tetrahydroquinolines

4. The Povarov Reaction as a Versatile Strategy for the Preparation of 1, 2, 3, 4-Tetrahydroquinoline Derivatives: An Overview

5. Synthesis of substituted 1,2,3,4-tetrahydroquinones by the Povarov reaction. New potentials of the classical reaction

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1. Accessing Tetrahydroquinaldic Amide and Homoproline Derivatives by Dearomative Difunctionalization of Heteroaromatics;Asian Journal of Organic Chemistry;2023-12-21

2. Transition‐Metal‐Free Regioselective Direct C2, C4 Difunctionalization and C2, C4, C6 Trifunctionalization of Pyridines;Advanced Synthesis & Catalysis;2022-07-14

3. Recent advances in the dearomative functionalisation of heteroarenes;Chemical Science;2022