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PubMed:24960214 JSONTXT

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NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T1 87-101 OrganismTaxon denotes Rhodococcus sp NCBItxid:1831
T2 198-212 OrganismTaxon denotes Rhodococcus sp NCBItxid:1831

GlyCosmos6-CLO

Id Subject Object Predicate Lexical cue
T1 284-294 http://purl.obolibrary.org/obo/CLO_0001658 denotes activation

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-102 Sentence denotes Chemical synthesis of a tetrasaccharide related to the exocellular polysaccharide from Rhodococcus sp.
TextSentencer_T2 103-108 Sentence denotes RHA1.
TextSentencer_T3 109-213 Sentence denotes Chemical synthesis of the tetrasaccharide related to the exocellular polysaccharide from Rhodococcus sp.
TextSentencer_T4 214-231 Sentence denotes RHA1 is reported.
TextSentencer_T5 232-447 Sentence denotes The stereoselective glycosylations were achieved by activation of the thioglycoside donors using N-iodosuccinimide in the presence of La(OTf)3 varying temperature per the need of 1,2-cis or 1,2-trans glycosylations.
TextSentencer_T6 448-680 Sentence denotes The target tetrasaccharide is reported in the form of its p-methoxyphenyl glycoside that can be cleaved selectively from the per-O-acetylated derivative allowing further glycoconjugate formation using trichloroacetimidate chemistry.
T1 0-102 Sentence denotes Chemical synthesis of a tetrasaccharide related to the exocellular polysaccharide from Rhodococcus sp.
T2 103-108 Sentence denotes RHA1.
T3 109-213 Sentence denotes Chemical synthesis of the tetrasaccharide related to the exocellular polysaccharide from Rhodococcus sp.
T4 214-231 Sentence denotes RHA1 is reported.
T5 232-447 Sentence denotes The stereoselective glycosylations were achieved by activation of the thioglycoside donors using N-iodosuccinimide in the presence of La(OTf)3 varying temperature per the need of 1,2-cis or 1,2-trans glycosylations.
T6 448-680 Sentence denotes The target tetrasaccharide is reported in the form of its p-methoxyphenyl glycoside that can be cleaved selectively from the per-O-acetylated derivative allowing further glycoconjugate formation using trichloroacetimidate chemistry.