28875-69-6Relevant academic research and scientific papers
Toward the stereoselective synthesis of zaragozic acid framework: A desilylation-aldol reaction approach
Castillón, Sergio,Kurniawan, Yudhi D.,Robinson, Andrea J.,Tuck, Kellie L.
supporting information, (2021/11/08)
A convergent synthesis of the C3-C8 fragment of zaragozic acids is described. The key reactions include desilylation-aldol reaction, rearrangement induced by regioselective reductive cleavage, BAIB/TEMPO-Pinnick oxidation, esterification, silylation, and hydrogenolysis.
Synthesis and stereochemistry of musacins isolated from Streptomyces griseoviridis (FH-S 1832)
Ueki, Toshihiko,Kinoshita, Takamasa
, p. 295 - 302 (2007/10/03)
Musacins E (1a), B1, (2a) and B2 (3a) have been synthesized starting from D-erythronolactone, L-tartaric acid and (S)-malic acid. The absolute stereochemistry of musacins was unambiguously established by this synthesis.
