Synthesis of cycloalkenones via the intramolecular cyclopropanation of furanyl diazo ketones
A Padwa, TJ Wisnieff, EJ Walsh
Index: Padwa, Albert; Wisnieff, Thomas J.; Walsh, Edward J. Journal of Organic Chemistry, 1986 , vol. 51, # 25 p. 5036 - 5038
Full Text: HTML
Citation Number: 24
Abstract
Summary: The reaction of a-diazo ketones derived from furanyl and benzofuranyl propionic acids with rhodium (I1) acetate leads to cycloalkenones in high yield. Mechanistically, the reaction involves addition of the keto carbene to the furanyl? r-bond followed by an electrocyclic ring opening reaction.
Related Articles:
Intramolecular cyclopropanation reaction of furanyl diazo ketones
[Padwa, Albert; Wisnieff, Thomas J.; Walsh, Edward J. Journal of Organic Chemistry, 1989 , vol. 54, # 2 p. 299 - 308]