Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 73, Issue 13, Pages 5183-5186Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo800594y
Keywords
-
Categories
Funding
- National Research Foundation of Korea [R01-2006-000-11283-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Ask authors/readers for more resources
4-Acetoxy-2-azetidinones reacted with organoindium reagent generated in situ from indium and 1,6-dibromo-2,4-hexadiyne in the presence of LiCl in DMF to selectively produce 2-azetidinones possessing 1,2,4,5-hexatetraen-3-yl group on the C4-position. The Diels-Alder reactions of 4-(1,2,4,5-hexatetraen-3-yl)-2-azetidinones with a variety of dienophiles and subsequent aromatizations afforded valuable functional group-substituted 2-azetidinones in good yields.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available