PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 28272765-5 2017 The new glycoside acceptors feature a picoloyl (Pico) protecting group at the remote C4/C3 position that confers unusual stability on TMS glycosides under acidic conditions. Glycosides 8-17 complement C4A (Rodgers blood group) Homo sapiens 85-90 28272765-5 2017 The new glycoside acceptors feature a picoloyl (Pico) protecting group at the remote C4/C3 position that confers unusual stability on TMS glycosides under acidic conditions. Glycosides 138-148 complement C4A (Rodgers blood group) Homo sapiens 85-90 14599211-5 2003 In the case of glycosaminoglycan-derived amidyl radicals, evidence has been obtained in studies with model glycosides that these radicals undergo rapid intramolecular abstraction reactions to give carbon-centered radicals at C-2 on the N-acetyl glycosamine rings (via a 1,2-hydrogen atom shift) and at C-4 on the neighboring uronic acid residues (via 1,5-hydrogen atom shifts). Glycosides 107-117 complement C4A (Rodgers blood group) Homo sapiens 302-305 14599211-6 2003 The C-4 carbon-centered radicals, and analogous species derived from model glycosides, undergo pH-independent beta-scission reactions that result in glycosidic bond cleavage. Glycosides 75-85 complement C4A (Rodgers blood group) Homo sapiens 4-7 861975-3 1977 Reduction of the ketone group at C-4 in the glycoside 13 with sodium borohydride afforded the corresponding methyl 6-O-benzyl-2,3-dideoxy-erythro-hex-2-enopyranosides (14). Glycosides 44-53 complement C4A (Rodgers blood group) Homo sapiens 33-36