157666-05-2Relevant articles and documents
Facile synthesis of 2-C-methyl-D-arabino-γ-1,4-lactones and mechanism study
Lv, Bingqing,Guo, Shuang,Zhu, Fuqiang,Hu, Tianwen,Guo, Qi,Lin, Haixia,Xie, Yuanchao,Shen, Jingshan
supporting information, p. 1473 - 1475 (2018/03/13)
In our previous research on the synthesis of 3,5-di-O-benzoyl-2-C-methyl-D-arabino-γ-lactone 4a, the reaction mechanism of DMSO-mediated configuration inversion of C2 hydroxyl group in the lactone was ambiguous. As a follow-up to this research, we used s
A NEW SYMTHESIS OF 2-C-METHYL-D-RIBONO-1,4-LACTONE AND THE C-9/C-13 FRAGMENT OF METHYNOLIDE
Lopez-Herrera, F. J.,Sarabia-Garcia, F.,Pino-Gonzalez, M. S.,Garcia-Aranda, J. F.
, p. 767 - 776 (2007/10/02)
The synthesis of the glucosaccharino lactone, 2-C-methyl-D-ribono-1,4-lactone 7 from 2,3-O-isopropylidene-D-glyceraldehyde 1 is reported.Lactone 7 was transformed into (2R,3R)-2,3-dihydroxy-2-methylpentanoic acid 18 (the C-9/C-13 fragment of Methynolid) b