121056-95-9Relevant articles and documents
Synthesis of the octahydroindole unit of aeruginosins via asymmetric hydrogenation of the Diels-Alder adducts of 2-amido-2,4-pentadienoate
Hoshina, Yoichiro,Doi, Takayuki,Takahashi, Takashi
, p. 12740 - 12746 (2007)
An optically active octahydroindole, the core unit of aeruginosins (Choi) was synthesized. The Diels-Alder reaction of Danishefsky's diene with methyl (Z)-2-acetamido-2,4-pentadienoates provided the adducts regioselectively in good yield. The adducts were
SYNTHESIS OF (S)-6-HYDROXYTRYPTOPHAN AND DERIVATIVES THEREOF
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, (2020/07/07)
The present invention relates to novel methods and compounds for synthesizing amanitin derivatives. The invention in particular relates to methods for synthesizing (S)-6-hydroxy-tryptophan derivatives which can be used as building blocks for synthesizing
Preparation of horner-wadsworth-emmons reagent: Methyl 2- benzyloxycarbonylamino-2-(dimethoxy-phosphinyl)acetate
Azuma, Hiroki,Okano, Kentaro,Fukuyama, Tohru,Tokuyama, Hidetoshi
, p. 152 - 161 (2014/04/03)
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