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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

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2009, Issue 5, Pages 730-738

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200800924

Keywords

Cyclotrimerization; Diels-Alder reaction; Diphenylalkanes; Diversity-oriented approach; Metathesis

Funding

  1. Department of Science & Technology (DST), New Delhi
  2. Sophisticated Analytical Instrument Facility (SAIF), Bombay
  3. Scientific & Industrial Research (CSIR), New Delhi

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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 alpha,omega-diyne scaffold to build functionalized aromatic units. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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