Annulation based on 8-aminoquinoline assisted C–H activation: an emerging tool in N-heterocycle construction-Reference-Cited by-同舟云学术

Annulation based on 8-aminoquinoline assisted C–H activation: an emerging tool in N-heterocycle construction

Published:2016 Issue:6 Volume:3 Page:768-772
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wan Jie-Ping¹²³⁴,Li Yi¹²³⁴,Liu Yunyun¹²³⁴

Affiliation:

1. College of Chemistry and Chemical Engineering

2. Jiangxi Normal University

3. Nanchang 330022

4. P. R. China

Abstract

As an important emerging area of 8-aminoquinoline assisted C–H activation, the construction of heterocycles via direct C–H activation and domino reactions involving domino C–H activation/annulation has been highlighted.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/QO/C6QO00077K

Reference24 articles.

1. Highly Regioselective Arylation of sp3 C−H Bonds Catalyzed by Palladium Acetate

2. 8-Aminoquinoline: A Powerful Directing Group in Metal-Catalyzed Direct Functionalization of CH Bonds

3. Catalytic Functionalization of C(sp2)H and C(sp3)H Bonds by Using Bidentate Directing Groups

4. Bidentate, Monoanionic Auxiliary-Directed Functionalization of Carbon–Hydrogen Bonds

5. Construction of N-containing heterocycles via oxidative intramolecular N–H/X–H coupling

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