38818-91-6Relevant academic research and scientific papers
Development of a new air-stable structure-simplified nafuredin-γ analog as a potent and selective nematode complex I inhibitor
Ohtawa, Masaki,Arima, Shiho,Shimizu, Risa,Hanatani, Naomi,Shimizu, Eri,Shiomi, Kazuro,Kita, Kiyoshi,ōmura, Satoshi,Nagamitsu, Tohru
, p. 647 - 654 (2017/05/29)
Nafuredin-γ, obtained from natural nafuredin, has demonstrated a potent and selective inhibitory activity against nematode complex I. However, nafuredin-γ is unstable in air since its conjugated dienes are oxygen-labile. The instability in air was natural
General preparation and controlled cyclization of acyclic terpenoids
Kuk, Jinchul,Beom, Soo Kim,Jung, Heejung,Choi, Seyoung,Park, Jung-Youl,Koo, Sangho
, p. 1991 - 1994 (2008/09/18)
A general preparation method of the all-(E)-polyprenols 12 has been developed from readily available geranyl sulfone by the chain-extension process utilizing the C5 unit 5 and the chain-termination process utilizing the C5 unit 10 to
Superacidic low temperature cyclization of terpenylphenyisulfones
Kulcitki, Veaceslav,Ungur, Nicon,Vlad, Pavel F.
, p. 11925 - 11934 (2007/10/03)
The superacidic cyclization of aliphatic and partially cyclized C10- C20 terpenylphenylsulfones proceeds structure-selectively and stereospecifically, affording α- or mixtures of α- and γ-isomers of completely cyclized terpenylphenylsulfones. The configuration of the phenylsuffonylmethylene group in the cyclized products is predetermined by the configuration of the allylic double bond in the starting compounds.
Tetra-n-butylammonium Oxone. Oxidations under Anhydrous Conditions
Trost, Barry M.,Braslau, Rebecca
, p. 532 - 537 (2007/10/02)
Tetra-n-butylammonium Oxone, readily prepared as a white solid from commercially available Oxone, performs oxidations in anhydrous methylene chloride.Under these conditions, sulfides are oxidized to sulfones in the presence of amines, ketones, esters, car
