Acetate → HCID 22472984, compound

HRID 168071Notes

Reaction equation

HRID 168071 reaction equation
[C:40]([O-:41])(=[O:42])[CH3:43].[C:45]([O-:46])(=[O:47])[CH3:48].[CH3:29][CH2:30][N:31]([CH2:32][CH3:33])[CH2:34][CH3:35].[CH3:36][S:37]([CH3:38])=[O:39].[Cu+2:44].[N+:1](=[O:2])([O-:3])[c:4]1[cH:5][cH:6][c:7]([O:10][c:11]2[cH:12][c:13]3[cH:14][n:15][nH:16][c:17]3[cH:18][cH:19]2)[n:8][cH:9]1.[n:20]1[cH:21][c:22]([B:26]([OH:27])[OH:28])[cH:23][cH:24][cH:25]1>>[N+:1](=[O:2])([O-:3])[c:4]1[cH:5][cH:6][c:7]([O:10][c:11]2[cH:12][c:13]3[cH:14][n:15][n:16](-[c:22]4[cH:21][n:20][cH:25][cH:24][cH:23]4)[c:17]3[cH:18][cH:19]2)[n:8][cH:9]1

Participants

7

Reactant 6

HCID 175Acetate2×HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 27099Cupric cationHCID 27343783-Pyridinylboronic acidHCID 22472992HCID 22472992, compound

Product 1

HCID 22472984HCID 22472984, compound

Sources & evidence

ORD record
ord-0512c1cbc70d4f10a0f5a14274741cd8
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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