921757-66-6Relevant articles and documents
A Scalable biomimetic synthesis of resveratrol dimers and systematic evaluation of their antioxidant activities
Matsuura, Bryan S.,Keylor, Mitchell H.,Li, Bo,Lin, Yuxuan,Allison, Shelby,Pratt, Derek A.,Stephenson, Corey R. J.
supporting information, p. 3754 - 3757 (2015/03/18)
An efficient synthetic route to the resveratrol oligomers quadrangularin A and pallidol is reported. It features a scalable biomimetic oxidative dimerization that proceeds in excellent yield and with complete regioselectivity. A systematic evaluation of t
Total synthesis of (±)-quadrangularin A
Li, Wenling,Li, Hao,Li, Ying,Hou, Zijie
, p. 7609 - 7611 (2008/02/12)
The key to successful coupling in the synthesis of (±)- quadrangularin A (1) was the introduction of tert-butyl groups in the precursor to block two reactive positions. Thus, the oxidative coupling of 3,5-di-(tert-butyl) resveratrol was carried out regioselectively in an efficient total synthesis of the natural product. (Chemical Equation Presented)
