Chappell, D. and Russell, A.T. (2006) From alpha-cedrene to crinipellin B and onward: 25 years of the alkene-arene meta-photocycloaddition reaction in natural product synthesis. Organic and Biomolecular Chemistry, 4 (24). pp. 4409-4430. ISSN 1477-0520 doi: 10.1039/b614011b
Abstract/Summary
Wender and Howbert's remarkable synthesis of alpha-cedrene in 1981 brought the attention of the synthetic community to the alkene - arene meta-photocycloaddition reaction. Here we review the natural product syntheses that have been achieved, over the last 25 years, utilising this strategic level reaction.
Altmetric Badge
| Item Type | Article |
| URI | https://reading-clone.eprints-hosting.org/id/eprint/11117 |
| Identification Number/DOI | 10.1039/b614011b |
| Refereed | Yes |
| Divisions | Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry |
| Uncontrolled Keywords | OLEFIN CYCLO-ADDITIONS, DONOR-ACCEPTOR SYSTEMS, AROMATIC-COMPOUNDS, CATIONIC REARRANGEMENTS, PHOTOCHEMICAL CYCLOADDITION, BICHROMOPHORIC MOLECULES, ORGANIC-PHOTOCHEMISTRY, SIMPLE DERIVATIVES, EXCIPLEX FORMATION, CHARGE-TRANSFER IVCT, SPECTROELECTROCHEMICAL PROPERTIES |
| Download/View statistics | View download statistics for this item |
University Staff: Request a correction | Centaur Editors: Update this record
Download
Download