Synthesis and Chemistry of 1H-Cyclobuta [de] naphthalenes, 1-Alkylidene-1H-cyclobuta [de] naphthalenes, and 1H-Cyclobuta [de] naphthalen-1-one
PJ Card, FE Friedli, H Shechter
Index: Card,P.J.; Friedli,F.E.; Shechter,H. Journal of the American Chemical Society, 1983 , vol. 105, p. 6104
Full Text: HTML
Citation Number: 10
Abstract
Abstract: Grignard and lithium reagents from 1-bromo-lH-cyclobuta [de] naphthalene (la) are converted by protonic acids, trimethylsilyl chloride, methyl iodide, carbon dioxide, acetyl chloride, and ethylene oxide to the corresponding lH-cyclobuta [de] naphthalene derivatives. Further, displacements of la by various nucleophiles (aluminohydrides, iodide, chloride, cyanide, azide, methoxide and thiophenoxide, triphenylphosphine, silver nitrate, acetate, ...
Related Articles:
Reductive cleavage of aryl oxazolines to benzaldehydes and substituted toluenes
[Meyers, A. I.; Himmelsbach, Richard J.; Reuman, Michael Journal of Organic Chemistry, 1983 , vol. 48, # 22 p. 4053 - 4058]
[Ma, Shengming; Negishi, Ei-Ichi Journal of the American Chemical Society, 1995 , vol. 117, # 23 p. 6345 - 6354]
[Brown, George R.; Foubister, Alan J. Synthesis, 1982 , # 12 p. 1036 - 1037]
[Journal of Molecular Catalysis A: Chemical, , vol. 366, p. 210 - 214]
Facile reductive dehalogenation of organic halides with nickel boride at ambient temperature
[Khurana, Jitender M.; Kumar, Sanjay; Nand, Bhaskara Canadian Journal of Chemistry, 2008 , vol. 86, # 11 p. 1052 - 1054]