Michael-type additions to α, β-enoyliron (cyclopentadienyl) dicarbonyl complexes and its application to β-lactam synthesis
I Ojima, HB Kwon
Index: Ojima, Iwao; Kwon, Hyok Boong Chemistry Letters, 1985 , p. 1327 - 1330
Full Text: HTML
Citation Number: 5
Abstract
Michael-type additions of amines and thiols to α, β-enoyliron (cyclopentadienyl) dicarbonyl complexes were carried out to give the corresponding new β-aminoalkanoyl-and β- thioalkanoyliron complexes in good to excellent yields. A β-aminoalkanoyliron complex was treated with bromine in the presence of triethylamine to give the expected β-lactam in an excellent yield.
Related Articles:
[Georg, Gunda; Durst, Tony Journal of Organic Chemistry, 1983 , vol. 48, # 12 p. 2092 - 2095]
[Georg, Gunda; Durst, Tony Journal of Organic Chemistry, 1983 , vol. 48, # 12 p. 2092 - 2095]
[Georg, Gunda; Durst, Tony Journal of Organic Chemistry, 1983 , vol. 48, # 12 p. 2092 - 2095]
[Georg, Gunda; Durst, Tony Journal of Organic Chemistry, 1983 , vol. 48, # 12 p. 2092 - 2095]
[Georg, Gunda; Durst, Tony Journal of Organic Chemistry, 1983 , vol. 48, # 12 p. 2092 - 2095]