Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-121 |
Sentence |
denotes |
One-pot alpha-glycosylation pathway via the generation in situ of alpha-glycopyranosyl imidates in N,N-dimethylformamide. |
TextSentencer_T2 |
122-303 |
Sentence |
denotes |
Divergent pathways are disclosed in the activation of 2-O-benzyl-1-hydroxy sugars by a reagent combination of CBr4 and Ph3P, all of which afford one-pot alpha-glycosylation methods. |
TextSentencer_T3 |
304-520 |
Sentence |
denotes |
When this reagent is used in CH2Cl2, the 1-hydroxy sugar is converted to the alpha-glycosyl bromide in a conventional way and leads to the one-pot alpha-glycosylation method based on a halide ion-catalytic mechanism. |
TextSentencer_T4 |
521-624 |
Sentence |
denotes |
In either DMF or a mixture of DMF and CHCl3, however, alternative alpha-glycosyl species are generated. |
TextSentencer_T5 |
625-855 |
Sentence |
denotes |
From the 1H and 13C NMR study of the products, as well as the reactions using Vilsmeier reagents [(CH3)2N+=CHX]X- (X=Br and Cl), these were identified as cationic alpha-glycopyranosyl imidates having either Br- or Cl- counter ion. |
TextSentencer_T6 |
856-1065 |
Sentence |
denotes |
The cationic alpha-glycosyl imidate (Br-), derived specifically in the presence of DMF, is more reactive than the alpha-glycosyl bromide and thus is responsible for the accelerated one-pot alpha-glycosylation. |
TextSentencer_T7 |
1066-1256 |
Sentence |
denotes |
The one-pot alpha-glycosylation methodology performed in DMF was assessed also with different types of acceptor substrates including tertiary alcohols and an anomeric mixture of 1-OH sugars. |
T1 |
0-121 |
Sentence |
denotes |
One-pot alpha-glycosylation pathway via the generation in situ of alpha-glycopyranosyl imidates in N,N-dimethylformamide. |
T2 |
122-303 |
Sentence |
denotes |
Divergent pathways are disclosed in the activation of 2-O-benzyl-1-hydroxy sugars by a reagent combination of CBr4 and Ph3P, all of which afford one-pot alpha-glycosylation methods. |
T3 |
304-520 |
Sentence |
denotes |
When this reagent is used in CH2Cl2, the 1-hydroxy sugar is converted to the alpha-glycosyl bromide in a conventional way and leads to the one-pot alpha-glycosylation method based on a halide ion-catalytic mechanism. |
T4 |
521-624 |
Sentence |
denotes |
In either DMF or a mixture of DMF and CHCl3, however, alternative alpha-glycosyl species are generated. |
T5 |
625-855 |
Sentence |
denotes |
From the 1H and 13C NMR study of the products, as well as the reactions using Vilsmeier reagents [(CH3)2N+=CHX]X- (X=Br and Cl), these were identified as cationic alpha-glycopyranosyl imidates having either Br- or Cl- counter ion. |
T6 |
856-1065 |
Sentence |
denotes |
The cationic alpha-glycosyl imidate (Br-), derived specifically in the presence of DMF, is more reactive than the alpha-glycosyl bromide and thus is responsible for the accelerated one-pot alpha-glycosylation. |
T7 |
1066-1256 |
Sentence |
denotes |
The one-pot alpha-glycosylation methodology performed in DMF was assessed also with different types of acceptor substrates including tertiary alcohols and an anomeric mixture of 1-OH sugars. |