| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-87 |
Sentence |
denotes |
Synthesis, structure, and conformation of the dilactone derivative of GD1b ganglioside. |
| T1 |
0-87 |
Sentence |
denotes |
Synthesis, structure, and conformation of the dilactone derivative of GD1b ganglioside. |
| TextSentencer_T2 |
88-329 |
Sentence |
denotes |
Treatment of DG1b, beta-Gal-(1----3)-beta-GalNAc-(1---- 4)-[alpha-Neu5Ac-(2----8)-alpha-Neu5Ac-(2---- 3)]-beta-Gal-(1----4)-beta-Glc-(1----1)-Cer, with dicyclohexylcarbodi-imide in anhydrous methyl sulfoxide affords 95-98% of GD1b-dilactone. |
| T2 |
88-329 |
Sentence |
denotes |
Treatment of DG1b, beta-Gal-(1----3)-beta-GalNAc-(1---- 4)-[alpha-Neu5Ac-(2----8)-alpha-Neu5Ac-(2---- 3)]-beta-Gal-(1----4)-beta-Glc-(1----1)-Cer, with dicyclohexylcarbodi-imide in anhydrous methyl sulfoxide affords 95-98% of GD1b-dilactone. |
| TextSentencer_T3 |
330-550 |
Sentence |
denotes |
The carboxyl groups of the two sialic acid units are involved in ester linkages, as proved by ammoniolysis and reduction which gave derivatives containing the amide of sialic acid and N-acetylneuraminulose, respectively. |
| T3 |
330-550 |
Sentence |
denotes |
The carboxyl groups of the two sialic acid units are involved in ester linkages, as proved by ammoniolysis and reduction which gave derivatives containing the amide of sialic acid and N-acetylneuraminulose, respectively. |
| TextSentencer_T4 |
551-804 |
Sentence |
denotes |
1H-N.m.r. spectroscopy showed that the lactone rings involved position 9 of the inner sialic acid and position 2 of the inner galactose and that the disialosyl chain is extended toward the -beta-Gal-(1 ----4)-beta-Glc- portion of the ganglioside moiety. |
| T4 |
551-804 |
Sentence |
denotes |
1H-N.m.r. spectroscopy showed that the lactone rings involved position 9 of the inner sialic acid and position 2 of the inner galactose and that the disialosyl chain is extended toward the -beta-Gal-(1 ----4)-beta-Glc- portion of the ganglioside moiety. |
