New Nitronate σ Complexes and the Mechanism of Nucleophilic Aromatic Photosubstitution Para to a Nitro Group
Author:
Affiliation:
1. Department of Chemistry, University of Nebraska at Kearney, Kearney, Nebraska 68849
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0602497
Reference25 articles.
1. Karapire, C.; Icli, S. InOrganic Photochemistry and Photobiology, 2nd ed.; Horspool, W., Lenci, F., Eds.; CRC Press: Boca Raton, 2004; Chapter 37, pp 37-1−37-14.
2. 1-(o-Nitrophenyl)-2,2,2-trifluoroethyl Ether Derivatives as Stable and Efficient Photoremovable Alcohol-Protecting Groups
3. Photolytic Cleavage of 1-(2-Nitrophenyl)ethyl Ethers Involves Two Parallel Pathways and Product Release Is Rate-Limited by Decomposition of a Common Hemiacetal Intermediate
4. Toward the Development of New Photolabile Protecting Groups That Can Rapidly Release Bioactive Compounds upon Photolysis with Visible Light
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