Abstract
Arylnitroso dienophiles exist in equilibrium with their dimeric counterparts, which in turn form stable bidentate complexes with scandium(III) triflate and react with cyclohexadiene to give the corresponding Diels-Alder adduct at the same rate as the normal thermal process.
| Original language | English |
|---|---|
| Pages (from-to) | 2072-2073 |
| Number of pages | 1 |
| Journal | Chemical Communications |
| Issue number | 18 |
| DOIs | |
| Publication status | Published - 2002 |
Keywords
- ACID
- C-NITROSOBENZENES
- CYCLOADDITIONS
- {CYCLOADDITIONS
- CYCLOPENTADIENE
- {CYCLOPENTADIENE
- OXIDATION
- {INVESTIGATIONS
- IRON
- IRON} {SALTS
- {OXIDATION
- {SALTS
- STRUCTURAL
- STRUCTURAL} {INVESTIGATIONS
- {STRUCTURAL} {INVESTIGATIONS
- IRON SALTS
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CCDC 177523: Experimental Crystal Structure Determination
Lightfoot, A. P. (Contributor), Pritchard, R. (Contributor), Wan, H. (Contributor), Warren, J. (Contributor) & Whiting, A. (Contributor), Cambridge Crystallographic Data Centre, 1 Jan 2002
DOI: 10.5517/cc5yqkc, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc5yqkc&sid=DataCite
Dataset
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CCDC 176704: Experimental Crystal Structure Determination
Lightfoot, A. P. (Contributor), Pritchard, R. (Contributor), Wan, H. (Contributor), Warren, J. (Contributor) & Whiting, A. (Contributor), Cambridge Crystallographic Data Centre, 1 Jan 2002
DOI: 10.5517/cc5xw42, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc5xw42&sid=DataCite
Dataset