Kotha, Sambasivarao ; Khedkar, Priti (2009) A diversity-oriented approach to diphenylalkanes by strategic utilization of [2+2+2] cyclotrimerization, cross-enyne metathesis and Diels-Alder reaction European Journal of Organic Chemistry, 2009 (5). pp. 730-738. ISSN 1434-193X
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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/ejoc.20...
Related URL: http://dx.doi.org/10.1002/ejoc.200800924
Abstract
A novel and efficient approach towards the synthesis of polysubstituted diphenylalkane derivatives have been demonstrated using a strategic combination of [2+2+2] cyclotrimerization, ethylene cross-enyne metathesis and Diels-Alder reaction as key steps. The strategy involves the stepwise functionalization of acetylenic termini of α, ω-diyne scaffold to build functionalized aromatic units.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to John Wiley and Sons. |
| Keywords: | Cyclotrimerization; Diels-Alder Reaction; Diphenylalkanes; Diversity-oriented Approach; Metathesis |
| ID Code: | 65200 |
| Deposited On: | 15 Oct 2011 11:46 |
| Last Modified: | 15 Oct 2011 11:46 |
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