Nickel-Catalyzed Facile [2+2+2] Cyclotrimerization of Unactivated Internal Alkynes to Polysubstituted Benzenes-Reference-Cited by-同舟云学术

Nickel-Catalyzed Facile [2+2+2] Cyclotrimerization of Unactivated Internal Alkynes to Polysubstituted Benzenes

Published:2016-12-01 Issue:1 Volume:12 Page:168-173
ISSN:1861-4728
Container-title:Chemistry - An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Xue Fei¹,Loh Ying Kai²,Song Xiaolu²,Teo Wei Jie¹,Chua J. Y. Darrence²³,Zhao Jin¹²,Hor T. S. Andy¹²⁴

Affiliation:

1. Department of Chemistry; National University of Singapore; 3 Science Drive 3 Singapore 117543 Singapore

2. Institute of Materials Research and Engineering; Agency for Science, Technology and Research; 2 Fusionopolis Way, Innovis Singapore 138634 Singapore

3. School of Chemical and Biomedical Engineering; Nanyang Technological University; 62 Nanyang Drive Singapore 637459 Singapore

4. Department of Chemistry; The University of Hong Kong, Pokfulam; Hong Kong SAR China

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Reference87 articles.

1. [2 + 2 + 2] Cycloadditions

2. Transition Metal Alkyne Complexes: Transition Metal-catalyzed Cyclotrimerization

3. Recent Advances in the Transition-Metal-Catalyzed Regioselective Approaches to Polysubstituted Benzene Derivatives

4. Transition Metal Catalyzed [2+2+2] Cycloaddition and Application in Organic Synthesis

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