127844-86-4Relevant academic research and scientific papers
An improved, practical synthesis of the derivatives of 1-O-acetyl-2-deoxy-2-hydroxymethyl-D-erythrooxetanose, a key sugar moiety for the synthesis of oxetanosyl-N-glycoside
Nagai,Kato,Takita,Nishiyama,Yamamura
, p. 7703 - 7710 (2007/10/02)
Intramolecular cyclization of the cis-epoxy-alcohol (6) with KOH in aq.DMSO provided predominantly the oxetane compound (7), which on oxidation followed by Baeyer-Villiger reaction gave 1-O-acetyl-D-erythrooxetanoses.
A FACILE AND PRACTICAL SYNTHESIS OF THE DERIVATIVES OF 1-O-ACETYL-2-DEOXY-2-HYDROXYMETHYL-D-ERYTHROOXETANOSE, A KEY SUGAR MOIETY FOR THE SYNTHESIS OF OXETANOSYL-N-GLYCOSIDE
Nagai, Masashi,Kato, Kuniki,Takita, Tomohisa,Nishiyama, Shigeru,Yamamura, Shosuke
, p. 119 - 120 (2007/10/02)
Intramolecular cyclization of the epoxy-alcohol (6) with KOH in aq.DMSO gave predominantly the oxetane compound (7), which could be transformed into some 1-O-acetyl-D-oxetanoses.
