Copper/Diethyl Azodicarboxylate Mediated Regioselective Alkynylation of Unactivated Aliphatic Tertiary Methylamine with Terminal Alkyne-Reference-Cited by-同舟云学术

Copper/Diethyl Azodicarboxylate Mediated Regioselective Alkynylation of Unactivated Aliphatic Tertiary Methylamine with Terminal Alkyne

Published:2009-01-21 Issue:4 Volume:11 Page:1027-1029
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xu Xiaoliang¹,Li Xiaonian¹

Affiliation:

1. Institute of Industrial Catalysis, College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310032, People’s Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol802974b

Reference40 articles.

1. Palladium-Catalyzed C−H Functionalization of Pyridine N-Oxides: Highly Selective Alkenylation and Direct Arylation with Unactivated Arenes

2. Functionalizing Glycine Derivatives by Direct CC Bond Formation

3. Ruthenium-Catalyzed Oxidative Cross-Coupling of Chelating Arenes and Cycloalkanes

4. The Catalytic Cross-Coupling of Unactivated Arenes

5. Catalytic and Highly Regioselective Cross-Coupling of Aromatic C−H Substrates

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