반응식
[C@H:1]1([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@H:17]([OH:20])[CH:18]=[O:19])[O:9][C@H:8]([CH2:10][OH:11])[C@@H:6]([OH:7])[C@H:4]([OH:5])[C@H:2]1[OH:3]>C(O)[C@H]1O[C@H](OC[C@H]2OC(O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O>[CH2:10]([OH:11])[C@H:8]1[O:9][C@H:1]([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@H:17]([OH:20])[CH2:18][OH:19])[C@H:2]([OH:3])[C@@H:4]([OH:5])[C@@H:6]1[OH:7].[CH2:10]([OH:11])[C@H:8]1[O:9][C@H:1]([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@@H:17]([OH:20])[CH2:18][OH:19])[C@H:2]([OH:3])[C@@H:4]([OH:5])[C@@H:6]1[OH:7].[CH2:10]([OH:11])[C@H:8]1[O:9][C@H:1]([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@@H:17]([OH:20])[CH2:18][OH:19])[C@H:2]([OH:3])[C@@H:4]([OH:5])[C@@H:6]1[OH:7]참가 물질
실험 절차
In the process according to the invention, the depletion of the epimerized mixture in isomaltose is, on the contrary, carried out in such a manner as to obtain a fraction containing a roughly equimolecular proportion of isomaltose and α-D-glucopyranosyl-(1→6)-D-mannose, the other fraction being constituted by very pure isomaltose. By roughly equimolecular is meant from 40 to 60% and more preferably from 45 to 55% of one of the two compounds relative to the total mass of the two compounds. This way of proceeding has the advantage of directly obtaining a mixture which after hydrogenation will provide the two components of palatinitol, namely isomaltitol and GPM in roughly equimolecular proportions, without having to resort to remixing pure fractions.
후처리
- customto obtain a fraction
- customof directly obtaining a mixture which after hydrogenation
출처 및 근거
- ORD 기록
- ord-19b8ce0752ca4c2b96638b594f446aff
- 출처 데이터셋
- uspto-grants-1999_01
- 특허 번호
- US05856469
연결된 노트
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