Copper- and Ligand-free Heteroannulation ofo-Halohydroxypyridine with Terminal Alkynes Using Pd/C Catalyst: One-Pot Synthesis of 2-Substituted Furopyridines and their Functionalization-Reference-Cited by-同舟云学术

Copper- and Ligand-free Heteroannulation ofo-Halohydroxypyridine with Terminal Alkynes Using Pd/C Catalyst: One-Pot Synthesis of 2-Substituted Furopyridines and their Functionalization

Published:2015-01 Issue:1 Volume:36 Page:211-218
ISSN:1229-5949
Container-title:Bulletin of the Korean Chemical Society
language:en
Short-container-title:Bull. Korean Chem. Soc

Author:

Park Hee Jung¹,Kim Ji-Eun²,Yum Eul Kgun²,Kim Young Hoon³,Han Chang-Woo³

Affiliation:

1. Western Seoul Center Korea Basic Science Institute; Seoul 120-750 Korea

2. Department of Chemistry; Chungnam National University; Daejon 305-764 Korea

3. High Tech Pharm. Co.; R&D Center; Eumseong 369-823 Korea

Funder

Korea Basic Science Institute (KBSI)

High Tech Pharm Co.

Publisher

Wiley

Subject

General Chemistry

Reference47 articles.

1. Diastereoselective multicomponent synthesis and anti-HSV-1 evaluation of dihydrofuran-fused derivatives

2. Furo[2,3-b]pyridine-based cannabinoid-1 receptor inverse agonists: Synthesis and biological evaluation. Part 1

4. Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases

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3. ChemInform Abstract: Copper- and Ligand-Free Heteroannulation of o-Halohydroxypyridine with Terminal Alkynes Using Pd/C Catalyst: One-Pot Synthesis of 2-Substituted Furopyridines and Their Functionalization.;ChemInform;2015-06