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A Diversity-Oriented Approach to Diphenylalkanes by Strategic Utilization of [2+2+2] Cyclotrimerization, Cross-Enyne Metathesis and Diels–Alder Reaction
✍ Scribed by Sambasivarao Kotha; Priti Khedkar
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 213 KB
- Volume
- 2009
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
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.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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## Abstract 7‐Oxanorbornene derivatives functionalized with alkyneappendages undergo intramolecular enyne metathesis reactions to give __cis__‐fused 2,6‐dioxabicyclo[4.3.0]nonane derivatives. These compounds have a diene functionality thatallows their reaction with dienophiles (__N__‐phenylmaleimid