We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Reductive Heck Reactions and [3+2] Cycloadditions of Unsaturated N,N'-Bistricyclic Imides.
- Authors
Gul, Melek; Kulu, Irem; Gunkara, Omer Tahir; Ocal, Nuket
- Abstract
The C-C coupling of N,N'-bis(5-norbornene-2,3-dicarboximide) (3) and N,N'-bis(7-oxa-5-norbornene-2,3-dicarboximide) (6) with aryl and heteroaryl iodides gave under reductive Heck conditions the C-aryl(hetaryl), substituted N,N'-bistricyclic imides 7a-f and 8a,b. The fused spiro-1,3-indandionolylpyrrolidine compounds, 9, 10 and 11 were also ob- tained from ninhydrine, sarcosine and 3 or 6 via [3+2]cycloaddition.
- Subjects
CHEMICAL reduction; CHEMICAL reactions; RING formation (Chemistry); IMIDES; COUPLING agents (Chemistry); DICARBOXIMIDES
- Publication
Acta Chimica Slovenica, 2013, Vol 60, Issue 1, p87
- ISSN
1318-0207
- Publication type
Article