Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
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Visible-Light-Mediated [4+2] Cycloaddition of Styrenes: Synthesis of Tetralin Derivatives.Biomimetic Total Synthesis of (±)-Griffipavixanthone via a Cationic Cycloaddition-Cyclization Cascade.Gnetin-C and other resveratrol oligomers with cancer chemopreventive potential.Polypharmacology or Promiscuity? Structural Interactions of Resveratrol With Its Bandwagon of TargetsSamarium(II) folding cascades involving hydrogen atom transfer for the synthesis of complex polycycles
P2860
Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
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2016 nî lūn-bûn
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Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
@en
Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
@nl
type
label
Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
@en
Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
@nl
prefLabel
Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
@en
Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium.
@nl
P2093
P2860
P50
P356
P1433
P1476
Synthesis of resveratrol tetramers via a stereoconvergent radical equilibrium
@en
P2093
Bryan S Matsuura
Derek A Pratt
Mariia S Kirillova
Mitchell H Keylor
Ryan A Harding
P2860
P304
P356
10.1126/SCIENCE.AAJ1597
P407
P577
2016-12-01T00:00:00Z