406179-91-7Relevant articles and documents
Synthesis of cyclic dienamide using ruthenium-catalyzed ring-closing metathesis of ene-ynamide.
Saito, Nozomi,Sato, Yukako,Mori, Miwako
, p. 803 - 805 (2002)
[reaction: see text] Ring-closing metathesis of ene-ynamide using the second-generation Grubbs' catalyst produced nitrogen-containing heterocycles, which have dienamide moieties, in high yields. Diels-Alder reaction of the cyclized product and dienophile
Synthesis of cyclic dienamide using ruthenium-catalyzed ring-closing metathesis of ene-ynamide
Mori, Miwako,Wakamatsu, Hideaki,Saito, Nozomi,Sato, Yukako,Narita, Rie,Sato, Yoshihiro,Fujita, Reiko
, p. 3872 - 3881 (2007/10/03)
Ring-closing metathesis of ene-ynamide, which has alkene and ynamide moieties in a molecule, using a second-generation ruthenium carbene complex produced nitrogen-containing heterocycles, which have a dienamide moiety, in high yields. Diels-Alder reaction
Synthesis of different ring-size heterocycles from the same propargyl alcohol derivative by ligand effect on Pd(0)
Kozawa, Yuji,Mori, Miwako
, p. 1499 - 1502 (2007/10/03)
The type of ligand on an allenylpalladium complex, which was prepared from propargyl alcohol derivative and Pd(0), plays an important role in determination of the ring size of the cyclized compound. An intermediary palladium complex bearing a monodentate ligand gave a cyclized compound via palladacycle, while that bearing a bidentate ligand gave one-carbon elongated cyclized compound via a η3-propargylpalladium complex.
