Journal
ORGANIC LETTERS
Volume 14, Issue 8, Pages 2184-2187Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol3008183
Keywords
-
Categories
Funding
- NSF [0844931]
- NIH [R01HL088559]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [0844931] Funding Source: National Science Foundation
Ask authors/readers for more resources
A reaction based fluorescence turn-on strategy for hydrogen sulfide (H2S) was developed. This strategy was based on a H2S-specific Michael addition-cyclization sequence. Other biological thiols such as cysteine and glutathione did not pursue the reaction and therefore did not turn on the fluorescence/consume the substrates. The probes showed good selectivity and sensitivity for hydrogen sulfide.
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
