Photofluorination of Aliphatic C–H Bonds Promoted by the Phthalimide Group
摘要:
Aliphatic C-H fluorination of phthalimide derivatives with Selectfluor was investigated under photo irradiation conditions. The reaction did not require any additive or catalyst and afforded C-H fluorinated products in moderate to good yields. It is likely that the reaction site depends on the C-H bond energy, and this may be the reason for the good to high regioselectivity.
Syntheses and Reactions of Acyclic N,N-Diacylglycines
作者:John C. Sheehan、Elias J. Corey
DOI:10.1021/ja01138a030
日期:1952.9
Ramer, Shawn E.; Moore, Richard N.; Vederas, John C., Canadian Journal of Chemistry, 1986, vol. 64, p. 706 - 713
作者:Ramer, Shawn E.、Moore, Richard N.、Vederas, John C.
DOI:——
日期:——
The Synthesis of Substituted Penicillins and Simpler Structural Analogs. VIII. Phthalimidomalonaldehydic Esters: Synthesis and Condensation with Penicillamine
作者:John C. Sheehan、David A. Johnson
DOI:10.1021/ja01630a043
日期:1954.1
Arrieta, A.; Garcia, T.; Lago, J. M., Synthetic Communications, 1983, vol. 13, # 6, p. 471 - 488