New amphiphilic glycopolymers by click functionalization of random copolymers – application to the colloidal stabilisation of polymer nanoparticles and their interaction with concanavalin A lectin

• Otman Otman,
• Paul Boullanger,
• Eric Drockenmuller and
• Thierry Hamaide

Beilstein J. Org. Chem. 2010, 6, No. 58, doi:10.3762/bjoc.6.58

• [1] whilst mannose units can be used for nerve cells targeting [2]. Besides naturally occurring polysaccharides, macromolecular engineering allows quite interesting possibilities for modelling of synthetic glycopolymers [3]. The hydrophobic component can be introduced by any convenient polymer moiety

Phaeochromycins F–H, three new polyketide metabolites from Streptomyces sp. DSS-18

• Jian Li,
• Chun-Hua Lu,
• Bao-Bing Zhao,
• Zhong-Hui Zheng and
• Yue-Mao Shen

Beilstein J. Org. Chem. 2008, 4, No. 46, doi:10.3762/bjoc.4.46

• was obtained by sodium dodecyl sulfate (SDS)-proteinase K lysis, selective precipitation of cell debris and polysaccharides with CTAB (hexadecyltrimethylammonium bromide), and isopropanol precipitation [9]. The bacterial strain was incubated on slope of GS media in a test tube at 28 °C for 5 d to