An Efficient Synthesis of Benzazocines by Gold(I)-Catalyzed Tandem 1,2-Acyloxy Shift/[3+2] Cycloaddition of Terminal 1,9-Enynyl Esters.

Chem Asian J

State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, 222 South Tianshui Road, Lanzhou, 730000, P. R. China.

Published: August 2016

An effective synthesis of structurally diverse benzazocines was accomplished in good to excellent chemical yields (55-82 %) through a gold(I)-catalyzed cascade reaction involving tandem 1,2-acyloxy shift/[3+2] cycloaddition of terminal 1,9-enynyl esters. The reaction proceeds under extremely mild conditions and represents one of the relatively few transition-metal-catalyzed intramolecular cycloaddition reactions for the synthesis of benzazocines.

Download full-text PDF

Source
http://dx.doi.org/10.1002/asia.201600593DOI Listing

Publication Analysis

Top Keywords

synthesis benzazocines
8
tandem 12-acyloxy
8
12-acyloxy shift/[3+2]
8
shift/[3+2] cycloaddition
8
cycloaddition terminal
8
terminal 19-enynyl
8
19-enynyl esters
8
efficient synthesis
4
benzazocines goldi-catalyzed
4
goldi-catalyzed tandem
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!