Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 79, Issue 3, Pages 846-851Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo402723e
Keywords
-
Categories
Funding
- Boehringer Ingelheim
- Bristol-Myers Squibb
- DuPont
- Eli Lilly
- Amgen
- AstraZeneca
- Roche
- A.P. Sloan Foundation
- S. T. Li Foundation
- Dreyfus Foundation
- University of California, Los Angeles
- Foote Family
- ACS Division of Organic Chemistry
- UCLA Graduate Division's DYF Program
Ask authors/readers for more resources
Heterocyclic arynes have long been targeted as potential tools for the synthesis of substituted heterocycles. Recent advances have led to an improved understanding of the factors that determine regioselectivity in reactions of these strained intermediates and, in turn, the aryne distortion model. This paper highlights the use of this predictive model to enable the use of heterocyclic arynes, such as indolynes and pyridynes, in chemical synthesis.
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