One-pot palladium-catalyzed highly chemo-, regio-, and stereoselective synthesis of trans-stilbene derivatives. A concise and convenient synthesis of resveratrol
T Jeffery, B Ferber
Index: Jeffery, Tuyet; Ferber, Benoit Tetrahedron Letters, 2003 , vol. 44, # 1 p. 193 - 197
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Citation Number: 68
Abstract
A convenient, efficient and highly chemo-, regio-, and stereoselective one-flask synthetic method is reported for the construction of unsymmetrical (or symmetrical) trans-stilbene derivatives based on two sequential Heck-type reactions using tetraalkylammonium salt- based catalyst systems and vinyltrimethylsilane as double bond equivalents. Resveratrol has thus been concisely synthesized.
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