145296-43-1Relevant academic research and scientific papers
Enantioselective total synthesis of (+)-serinolamide A
Gahalawat, Suraksha,Pandey, Satyendra Kumar
, p. 41013 - 41016 (2015/05/20)
A short and highly efficient enantioselective synthetic approach to (+)-serinolamide A 1 from racemic butadiene monoepoxide as a starting material is described. The synthesis utilizes the palladium catalyzed Trost's Dynamic Kinetic Asymmetric Transformation (DYKAT) and cross-metathesis (CM) as key steps.
A short and efficient synthesis of (2S,3S,4S)-tert-butyl 3,4-dihydroxy-2-(methoxymethyl)-5-oxopyrrolidine-1-carboxylate
Passiniemi, Mikko,Koskinen, Ari M.P.
experimental part, p. 2816 - 2822 (2010/10/04)
Asymmetric synthesis of the title compound was accomplished starting from l-serine. Stannoxane-mediated lactamization provided the key intermediate in good yield. Georg Thieme Verlag Stuttgart.
Synthesis of an enantiomerically pure serine-derived thiazole
Sowinski, Jennifer A.,Toogood, Peter L.
, p. 7671 - 7676 (2007/10/03)
Previously reported methods for preparing enantiomerically pure thiazoles are inadequate for the synthesis of inherently labile O-alkyl serine-derived thiazoles. The intermediate N-Boc-(O-methylseryl) thiazolines are very susceptible to tautomerization, e
