34311-63-2Relevant articles and documents
Dimerization of aldosuloses and aldonolactones into branched higher carbon sugars
Zhao, Yachen,Wang, Shengyang,Yu, Biao
supporting information, p. 2020 - 2022 (2020/02/22)
Homo-dimerizations of a variety of aldosulose and aldonolactone derivatives via aldol and Claisen reactions have been achieved, leading to novel branched higher carbon sugars in a highly stereoselective manner.
O-acetyl-ADP-ribose non-hydrolyzable analogs
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Page/Page column 10-11, (2010/11/28)
Compounds, compositions and methods for modulating cell death in target cells, particularly cancer cells are provided. The compounds are analogs of O-acetyl-ADP-ribose (OAADPr).
(3R,4S)-3,4,5-Trihydroxy-4-methylpentylphosphonic acid, an isosteric phosphonate analogue of 2-C-methyl-D-erythritol 4-phosphate, a key intermediate in the new pathway for isoprenoid biosynthesis
Hirsch, Guillaume,Grosdemange-Billiard, Catherine,Tritsch, Denis,Rohmer, Michel
, p. 519 - 521 (2007/10/03)
2-C-Methyl-D-erythritol 4-phosphate (MEP) is the first intermediate in the mevalonate-independent pathway for isoprenoid biosynthesis presenting the branched C5 isoprene skeleton. Enantiopure (3R,4S)-3,4,5-trihydroxy- 4-methylpentylphosphonic a