Heterobicyclic Core Retained Hydroarylations through C–H Activation: Synthesis of Epibatidine Analogues-Reference-Cited by-同舟云学术

Heterobicyclic Core Retained Hydroarylations through C–H Activation: Synthesis of Epibatidine Analogues

Published:2018-03-20 Issue:7 Volume:20 Page:2028-2032
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Deng-Yuan¹,Huang Zheng-Lu¹,Liu Pei-Nian¹^ORCID

Affiliation:

1. Shanghai Key Laboratory of Functional Materials Chemistry, Key Lab for Advanced Materials and School of Chemistry & Molecular Engineering, East China University of Science & Technology, Meilong Road 130, Shanghai 200237, China

Funder

Ministry of Education of the People's Republic of China

China Postdoctoral Science Foundation

Shanghai Municipal Education Commission

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b00571

Reference86 articles.

1. Epibatidine: a novel (chloropyridyl)azabicycloheptane with potent analgesic activity from an Ecuadoran poison frog

2. Alkaloids from Amphibian Skin: A Tabulation of Over Eight-Hundred Compounds

3. Using Physical Chemistry To Differentiate Nicotinic from Cholinergic Agonists at the Nicotinic Acetylcholine Receptor

4. Neuronal Nicotinic Acetylcholine Receptors: Structural Revelations, Target Identifications, and Therapeutic Inspirations

5. Varenicline: An α4β2 Nicotinic Receptor Partial Agonist for Smoking Cessation

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