Copper-Catalyzed Tandem Azide–Alkyne Cycloaddition, Ullmann Type C–N Coupling, and Intramolecular Direct Arylation-Reference-Cited by-同舟云学术

Copper-Catalyzed Tandem Azide–Alkyne Cycloaddition, Ullmann Type C–N Coupling, and Intramolecular Direct Arylation

Published:2013-08-16 Issue:17 Volume:15 Page:4304-4307
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Pericherla Kasiviswanadharaju¹,Jha Amitabh¹,Khungar Bharti¹,Kumar Anil¹

Affiliation:

1. Department of Chemistry, Birla Institute of Technology and Science, Pilani, 333031, India, and Department of Chemistry, Acadia University, Wolfville, NS, B4P 2R6, Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol401655r

Reference35 articles.

1. Metal-Catalyzed Cross-Coupling Reactions

2. Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis

3. Recent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formation

4. Transition-metal catalyzed oxidative cross-coupling reactions to form C–C bonds involving organometallic reagents as nucleophiles

5. Bond Formations between Two Nucleophiles: Transition Metal Catalyzed Oxidative Cross-Coupling Reactions

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