Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-86 |
Sentence |
denotes |
1,5-Anhydro-D-fructose; a versatile chiral building block: biochemistry and chemistry. |
TextSentencer_T2 |
87-277 |
Sentence |
denotes |
There is a steadily increasing need to expand sustainable resources, and carbohydrates are anticipated to play an important role in this respect, both for bulk and fine chemical preparation. |
TextSentencer_T3 |
278-358 |
Sentence |
denotes |
The enzyme alpha-(1-->4)-glucan lyase degrades starch to 1,5-anhydro-D-fructose. |
TextSentencer_T4 |
359-601 |
Sentence |
denotes |
This compound, which has three different functional properties, a prochiral center together with a permanent pyran ring, renders it a potential chiral building block for the synthesis of valuable and potentially biologically active compounds. |
TextSentencer_T5 |
602-705 |
Sentence |
denotes |
1,5-Anhydro-D-fructose is found in natural materials as a degradation product of alpha-(1-->4)-glucans. |
TextSentencer_T6 |
706-828 |
Sentence |
denotes |
The occurrence of lyases and the metabolism of 1,5-anhydro-D-fructose are reviewed in the biological part of this article. |
TextSentencer_T7 |
829-1036 |
Sentence |
denotes |
In the chemical part, the elucidated structure of 1,5-anhydro-D-fructose will be presented together with simple stereoselective conversions into hydroxy/amino 1,5-anhydro hexitols and a nojirimycin analogue. |
TextSentencer_T8 |
1037-1195 |
Sentence |
denotes |
Synthesis of 6-O-acylated derivatives of 1,5-anhydro-D-fructose substituted with long fatty acid residues is carried out using commercially available enzymes. |
TextSentencer_T9 |
1196-1268 |
Sentence |
denotes |
Those reactions lead to compounds with potential emulsifying properties. |
TextSentencer_T10 |
1269-1387 |
Sentence |
denotes |
The use of protected derivatives of 1,5-anhydro-D-fructose for the synthesis of natural products is likewise reviewed. |
TextSentencer_T11 |
1388-1474 |
Sentence |
denotes |
The potential utilization of this chemical building block is far from being exhausted. |
TextSentencer_T12 |
1475-1806 |
Sentence |
denotes |
Since 1,5-anhydro-D-fructose now is accessible in larger amounts through a simple-enzyme catalyzed degradation of starch by alpha-(1-->4)-glucan lyase, the application of 1,5-anhydro-D-fructose may be considered a valuable contribution to the utilization of carbohydrates as the most abundant resource of sustainable raw materials. |
T1 |
0-86 |
Sentence |
denotes |
1,5-Anhydro-D-fructose; a versatile chiral building block: biochemistry and chemistry. |
T2 |
87-277 |
Sentence |
denotes |
There is a steadily increasing need to expand sustainable resources, and carbohydrates are anticipated to play an important role in this respect, both for bulk and fine chemical preparation. |
T3 |
278-358 |
Sentence |
denotes |
The enzyme alpha-(1-->4)-glucan lyase degrades starch to 1,5-anhydro-D-fructose. |
T4 |
359-601 |
Sentence |
denotes |
This compound, which has three different functional properties, a prochiral center together with a permanent pyran ring, renders it a potential chiral building block for the synthesis of valuable and potentially biologically active compounds. |
T5 |
602-705 |
Sentence |
denotes |
1,5-Anhydro-D-fructose is found in natural materials as a degradation product of alpha-(1-->4)-glucans. |
T6 |
706-828 |
Sentence |
denotes |
The occurrence of lyases and the metabolism of 1,5-anhydro-D-fructose are reviewed in the biological part of this article. |
T7 |
829-1036 |
Sentence |
denotes |
In the chemical part, the elucidated structure of 1,5-anhydro-D-fructose will be presented together with simple stereoselective conversions into hydroxy/amino 1,5-anhydro hexitols and a nojirimycin analogue. |
T8 |
1037-1195 |
Sentence |
denotes |
Synthesis of 6-O-acylated derivatives of 1,5-anhydro-D-fructose substituted with long fatty acid residues is carried out using commercially available enzymes. |
T9 |
1196-1268 |
Sentence |
denotes |
Those reactions lead to compounds with potential emulsifying properties. |
T10 |
1269-1387 |
Sentence |
denotes |
The use of protected derivatives of 1,5-anhydro-D-fructose for the synthesis of natural products is likewise reviewed. |
T11 |
1388-1474 |
Sentence |
denotes |
The potential utilization of this chemical building block is far from being exhausted. |
T12 |
1475-1806 |
Sentence |
denotes |
Since 1,5-anhydro-D-fructose now is accessible in larger amounts through a simple-enzyme catalyzed degradation of starch by alpha-(1-->4)-glucan lyase, the application of 1,5-anhydro-D-fructose may be considered a valuable contribution to the utilization of carbohydrates as the most abundant resource of sustainable raw materials. |