Acetate → HCID 29153134, compound

HRID 298449Notes

Reaction equation

HRID 298449 reaction equation
[C:20](=[O:21])([O-:22])[O-:23].[CH3:10][c:11]1[n:12][o:13][c:14]([CH3:19])[c:15]1[B:16]([OH:17])[OH:18].[I:1][c:2]1[n:3][c:4]([S:8][CH3:9])[n:5][cH:6][cH:7]1.[Na+:24].[Na+:25].[O-:46][C:47]([CH3:48])=[O:49].[O-:50][C:51]([CH3:52])=[O:53].[Pd+2:45].[c:26]1([P:27]([c:28]2[cH:29][cH:30][cH:31][cH:32][cH:33]2)[c:34]2[cH:35][cH:36][cH:37][cH:38][cH:39]2)[cH:40][cH:41][cH:42][cH:43][cH:44]1>>[c:2]1(-[c:15]2[c:11]([CH3:10])[n:12][o:13][c:14]2[CH3:19])[n:3][c:4]([S:8][CH3:9])[n:5][cH:6][cH:7]1

Participants

8

Reactant 7

HCID 175Acetate2×HCID 923Sodium ion2×HCID 11776TriphenylphosphineHCID 19660Carbonate IonHCID 105144Allyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)HCID 27343463,5-Dimethylisoxazole-4-boronic acidHCID 38589014-Iodo-2-(methylthio)pyrimidine

Product 1

HCID 29153134HCID 29153134, compound

Sources & evidence

ORD record
ord-f2094539747d46208794c9ea38ffa291
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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