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Allyl bromide → 1-[tert-butyl(dimethyl)silyl]-4-oxo-3-prop-2-enylazetidine-2-carboxylic acid

HRID 2312530
Notes
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Reaction equation

HRID 2312530 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[Si:5]([N:6]1[CH:7]([C:11](=[O:12])[OH:13])[CH2:8][C:9]1=[O:10])([CH3:14])[CH3:15].[CH2:26]([CH:27]=[CH2:28])[Br:29].[CH2:30]1[O:31][CH2:32][CH2:33][CH2:34]1.[CH3:17][Si:18]([N-:19][Si:20]([CH3:21])([CH3:22])[CH3:23])([CH3:24])[CH3:25].[Li+:16]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[Si:5]([N:6]1[CH:7]([C:11](=[O:12])[OH:13])[CH:8]([CH2:28][CH:27]=[CH2:26])[C:9]1=[O:10])([CH3:14])[CH3:15]
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 7841Allyl bromideHCID 8028TetrahydrofuranHCID 28486Lithium CationHCID 3280088Npc316347HCID 34967161-(Tert-butyldimethylsilyl)-4-oxoazetidine-2-carboxylic acid

Product 1

HCID 1784397911-[tert-butyl(dimethyl)silyl]-4-oxo-3-prop-2-enylazetidine-2-carboxylic acid

Sources & evidence

ORD record
ord-1c6c1e58e0bb4a628010ec10d3fe9165
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes