16714-07-1Relevant articles and documents
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Stout et al.
, p. 1331,1332, 1334, 1335 (1975)
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Synthesis and membranoprotective properties of new disulfides with monoterpene and carbohydrate fragments
Pestova,Izmestev,Shevchenko,Rubtsova,Kuchin
, p. 723 - 731 (2015/11/27)
A cooxidation of carbohydrate and terpene thiols gives mixtures of disulfides containing 51 - 90% of the unsymmetric product. Membranoprotective and antioxidant properties of obtained unsymmetric and symmetric disulfides were evaluated based on their ability to inhibit the H2O2-induced hemolysis of erythrocytes, as well as the accumulation of secondary products of the peroxy oxidation of lipids and the oxidation of hemoglobin.
Umpolung reactivity in the stereoselective synthesis of S-linked 2-deoxyglycosides
Baryal, Kedar N.,Zhu, Danyang,Li, Xiaohua,Zhu, Jianglong
, p. 8012 - 8016 (2013/08/23)
Take control! An unprecedented sulfenylation of stereochemically defined 2-deoxyglycosyl lithium species with asymmetric sugar-derived disulfide acceptors enabled the stereoselective synthesis of both α- and β-S-linked 2-deoxyoligosaccharides. Reductive lithiation of 2-deoxyglycosyl phenylsulfides at -78°C provides predominantly axial glycosyl lithium species, which upon warming isomerize to predominantly equatorial lithium species (see scheme). Copyright