Journal
TETRAHEDRON LETTERS
Volume 56, Issue 1, Pages 32-52Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2014.11.061
Keywords
Propargylic amides; Transition-metal-catalyzed cyclization; Electrophilic cyclization
Categories
Funding
- National Natural Science Foundation of China [21172218]
Ask authors/readers for more resources
Cyclization reactions of propargylic amides, due to their rapid assembly of structural complexity and good functional group compatibility, have gained considerable attention in recent years. These transformations have been successfully achieved with transition metals, halogen sources, Bronsted acids, and strong bases. Generally, the cyclizations proceed through a 5-exo-dig or 6-endo-dig fashion to furnish heterocycles. (C) 2014 Published by Elsevier Ltd.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
