Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 43, 2013 - Issue 23
535
Views
8
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis of Pterostilbene by Julia Olefination

, &
Pages 3217-3223 | Received 21 Dec 2012, Published online: 04 Sep 2013

REFERENCES

  • Mizuno , C. S. ; Ma , G. ; Khan , S. ; Patny , A. ; Avery , M. A. ; Rimando , A. M. Design, synthesis, biological evaluation, and docking studies of pterostilbene analogs inside PPARalpha . Bioorg. Med. Chem. 2008 , 16 ( 7 ), 3800 – 3808 .
  • Stivala , L. A. ; Savio , M. ; Carafoli , F. ; Perucca , P. ; Bianchi , L. ; Maga , G. ; Forti , L. ; Pagnoni , U. M. ; Albini , A. ; Prosperi , E. ; Vannini , V. Specific structural determinants are responsible for the antioxidant activity and the cell cycle effects of resveratrol . J. Biol. Chem. 2001 , 276 ( 25 ), 22586 – 22594 .
  • Kimura , Y. ; Okuda , H. ; Arichi , S. Effects of stilbenes on arachidonate metabolism in leukocytes . Biochim. Biophys. Acta 1985 , 834 ( 2 ), 275 – 278 .
  • Mahady , G. B. ; Pendland , S. L. ; Chadwick , L. R. Resveratrol and red wine extracts inhibit the growth of CagA + strains of Helicobacter pylori in vitro . Am. J. Gastroenterol. 2003 , 98 ( 6 ), 1440 – 1441 .
  • Fremont , L. Biological effects of resveratrol . Life Sciences 2000 , 66 ( 8 ), 663 – 673 .
  • Spath , E. ; Kromp , K. Constituents of red sandalwood, III: Synthesis of pterostilbene . Ber. Dtsch. Chem. Ges. 1941 , 74B , 189 – 192 .
  • Sinha , A. K. ; Kumar , V. ; Sharma , A. ; Sharma , A. ; Kumar , R. An unusual, mild, and convenient one-pot, two-step access to (E)-stilbenes from hydroxy-substituted benzaldehydes and phenylacetic acids under microwave activation: A new facet of the classical Perkin reaction . Tetrahedron 2007 , 63 ( 45 ), 11070 – 11077 .
  • Moro , A. V. ; Cardoso , F. S. P. ; Correia , C. R. D. Heck arylation of styrenes with arenediazonium salts: Short, efficient, and stereoselective synthesis of resveratrol, DMU-212, and analogues . Tetrahedron Lett. 2008 , 49 ( 39 ), 5668 – 5671 .
  • Green , A. P. ; Hardy , S. ; Lee , A. T. L. ; Thomas , E. J. Approaches to the total synthesis of biologically active natural products: Studies directed towards bryostatins . Phytochemistry Rev. 2010 , 9 ( 4 ), 501 – 513 .
  • Killian , J. ; Abbe , T. ; Goess , B. Two routes to resveratrol: An exercise in synthesis planning and optimization for the advanced organic chemistry laboratory. In Abstracts, 63rd Southeast Regional Meeting of the American Chemical Society, Richmond, VA, United States, October 26–29, 2011; American Chemical Society: Washington, DC, pp. SERM-382.
  • Gupta , D. ; Singh , J. Triperpenoid saponins from centipede minima. Phytochemistry 1990, 29(6), 1945–1950.
  • Barrero , A. F. ; Herrador , M. M. ; Quilez del Moral , J. F. ; Arteaga , P. ; Akssira , M. ; Hanbali , F. E. ; Arteaga , J. F. ; Dieguez , H. R. ; Sanchez , E. M. Couplings of bezylic halides mediated by titanocene chloride: Synthesis of bibenzyl derivatives . J. Org. Chem. 2007 , 72 , 2251 – 2254 .
  • Ko , H. M. ; Lee , D. G. ; Kim , M. A. ; Kim , H. J. ; Park , J. ; Lah , M. S. ; Lee , E. Stereoselective synthesis of (−)-blepharocalyxin D . Tetrahedron 2007 , 63 , 5797 – 5805 .
  • Williams , D. R. ; Shamim , K. Efforts toward the total synthesis of (−)-kendomycin . Org. Lett. 2005 , 7 ( 19 ), 4161 – 4164 .

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.