Journal
ORGANIC LETTERS
Volume 17, Issue 9, Pages 2126-2129Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b00716
Keywords
-
Categories
Funding
- NIGMS CMLD initiative [P50 GM067041]
- Boston University Undergraduate Research Opportunities Program (UROP)
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1156666] Funding Source: National Science Foundation
Ask authors/readers for more resources
Cyclization of 1,6-diynes promoted by stoichiometric Ga(III) halides produces vinyl halides in good to excellent yields. Under acidic conditions, initially formed iodocyclization products undergo in situ Friedel-Crafts cyclizations, giving access to iodoindenopyridines. Application of the vinyl halides in cross-coupling reactions has been explored, and mechanistic aspects of the cyclization are discussed.
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
