Acetate → HCID 58515063, compound

HRID 688971Notes

Reaction equation

[Cl:1][c:2]1[n:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]2[cH:10][c:11]1[CH2:12][OH:13].[O-:45][C:46]([CH3:47])=[O:48].[O-:49][C:50]([CH3:51])=[O:52].[OH2:43].[Pd+2:44].[c:14]1([P:15]([c:16]2[cH:17][cH:18][cH:19][cH:20][cH:21]2)[c:22]2[cH:23][cH:24][cH:25][cH:26][cH:27]2)[cH:28][cH:29][cH:30][cH:31][cH:32]1.[c:33]1([CH3:42])[c:34]([B:39]([OH:40])[OH:41])[cH:35][cH:36][cH:37][cH:38]1>>[c:2]1(-[c:34]2[c:33]([CH3:42])[cH:38][cH:37][cH:36][cH:35]2)[n:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]2[cH:10][c:11]1[CH2:12][OH:13]

Participants

Reactant 6

HCID 175Acetate2×

HCID 962Water

HCID 11776Triphenylphosphine

HCID 105144Allyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)

HCID 930708(2-chloroquinolin-3-yl)methanol

HCID 27332672-Methylphenyl boronic acid

Product 1

HCID 58515063HCID 58515063, compound

Sources & evidence

ORD record: ord-4f6d39251c074247b9971ccb18fa5365
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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