HCID 53974377, compound → HCID 86600467, compound

HRID 400085Notes

Reaction equation

HRID 400085 reaction equation
[C:1]([O:18][CH2:19][C@H:20]1[O:26][CH:24]([OH:25])[C@H:23]([OH:27])[C@@H:22]([OH:28])[C@H:21]1[OH:29])(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>C(O)C>[C:1]([O:18][CH2:19][C@H:20]1[O:26][CH:24]([OH:25])[C@H:23]([OH:27])[C@@H:22]([OH:28])[C@H:21]1[OH:29])(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[O:18]=[CH:19][C@@H:20]([C@H:21]([C@H:22]([C@@H:23]([CH2:24][OH:25])[OH:27])[OH:28])[OH:29])[OH:26]

Participants

3

Reactant 1

HCID 53974377HCID 53974377, compound

Product 1

HCID 86600467HCID 86600467, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The procedure of (i) was repeated using 6-O-palmitoyl-D-galactopyranose (0.50 g) dissolved in ethanol (6 g).

Sources & evidence

ORD record
ord-9704b67a531d40588a79fcf7c86a9858
Source dataset
uspto-grants-1998_10
Patent number
US05827502

Reaction notes

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