Photosensitized oxidations of substituted pyrroles: Unanticipated radical-derived oxygenated products
MN Alberti, GC Vougioukalakis…
Index: Journal of Organic Chemistry, , vol. 74, # 19 p. 7274 - 7282
Full Text: HTML
Citation Number: 25
Abstract
... The Journal of Organic ... J. Org. Chem. ... Specifically, these products are obtained when a hydrogen atom(18a, 19) or an alkyl group(19c, 20) is placed at the α-position of the reactant pyrrole.(19c, 20) Furthermore, the oxygenation of organic compounds photosensitized by 9,10 ...
Related Articles:
[Deng, Guohua; Chen, Yongming Macromolecules, 2004 , vol. 37, # 1 p. 18 - 26]
A thermally-cleavable linker for solid-phase synthesis
[Keller, Keith A.; Guo, Jianhua; Punna, Sreenivas; Finn Tetrahedron Letters, 2005 , vol. 46, # 7 p. 1181 - 1184]
[Steele, Terry W. J.; Shier, Wayne Thomas Pharmaceutical Research, 2010 , vol. 27, # 4 p. 683 - 698]
Synthesis and antimicrobial activities of N-substituted imides
[Zentz, Frederic; Valla, Alain; Le Guillou, Regis; Labia, Roger; Mathot, Anne-Gabrielle; Sirot, Danielle Farmaco, 2002 , vol. 57, # 5 p. 421 - 426]