108907-43-3Relevant articles and documents
General synthesis of epi-series catechins and their 3-gallates: Reverse polarity strategy
Ohmori, Ken,Yano, Takahisa,Suzuki, Keisuke
supporting information; experimental part, p. 2693 - 2696 (2010/08/21)
A general synthetic route to the epi-series catechins was developed based on the reverse polarity strategy. Aromatic nucleophilic substitution reaction followed by the sulfinyl-metal exchange and cyclization enabled stereo-controlled access to various members of epi-series catechins and their 3-gallates.
PROANTHOCYANIDINS OF Rhodiola semenovii
Khi, Kim Khvan,Kuliev, Z. A.,Vdovin, A. D.,Yagudaev, M. R.,Malikov, V. M.
, p. 681 - 685 (2007/10/02)
The structures of two compounds previously isolated from Rhodiola semenovii, rhodokhinoside (I) and rhodikhim (II), have been established.