87030-12-4Relevant 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.
Total Synthesis of (+/-)- and (+)-Latifine
Takano, Seicchi,Akiyama, Masashi,Ogasawara, Kunio
, p. 2447 - 2454 (2007/10/02)
Racemic latifine (+)-(1), a new representative of the rare phenolic Amaryllidaceae alkaloids, has been synthesized by employing the Claisen rearrangement of 4-benzyloxycinnamyl 2-methoxyphenyl ether (11) as a key step.Based on the racemic synthesis, (R)-(
