Gold-Catalyzed Sequential Alkyne Activation: One-Pot Synthesis of NH-Carbazoles via Cascade Hydroarylation of Alkyne/6-Endo-Dig Carbocyclization Reactions-Reference-Cited by-同舟云学术

Gold-Catalyzed Sequential Alkyne Activation: One-Pot Synthesis of NH-Carbazoles via Cascade Hydroarylation of Alkyne/6-Endo-Dig Carbocyclization Reactions

Published:2013-06-21 Issue:13 Volume:78 Page:6769-6774
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Samala Srinivas,Mandadapu Anil K.,Saifuddin Mohammad,Kundu Bijoy¹

Affiliation:

1. Academy of Scientific and Innovative Research, New Delhi 110001, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo400799b

Reference45 articles.

1. Gold Catalysis

2. Gold-Catalysis: Highly Efficient and Regio-Selective Carbonyl Migration in Alkynyl-Substituted Indole-3-Carboxamides Leading to Azepino[3,4-b]indol-1-ones

3. A Diversity-Oriented Approach to Spiroindolines: Post-Ugi Gold-Catalyzed Diastereoselective Domino Cyclization

4. Enantioselective Gold-Catalyzed Synthesis of Polycyclic Indolines

5. Synthesis of the tetracyclic core skeleton of the lundurines by a gold-catalyzed cyclization

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