Acetate → HCID 22472972, compound

HRID 177483Notes

Reaction equation

HRID 177483 reaction equation
[C:41]([O-:42])(=[O:43])[CH3:44].[C:46]([O-:47])(=[O:48])[CH3:49].[CH3:30][CH2:31][N:32]([CH2:33][CH3:34])[CH2:35][CH3:36].[CH3:37][S:38]([CH3:39])=[O:40].[Cu+2:45].[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.[OH:20][B:21]([OH:22])[c:23]1[cH:24][cH:25][c:26]([F:27])[cH:28][cH:29]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:23]4[cH:24][cH:25][c:26]([F:27])[cH:28][cH:29]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 2856454-Fluorophenylboronic acidHCID 22472992HCID 22472992, compound

Product 1

HCID 22472972HCID 22472972, compound

Sources & evidence

ORD record
ord-d591921c7aec403486226d9913342b43
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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