Citric Acid → Tert-butyl 4-(2-(tert-butoxycarbonylamino)phenyl)-2-nitrobenzoate
Reaction equation
[Br:30][c:31]1[cH:32][c:33]([N+:44](=[O:45])[O-:46])[c:34]([C:35](=[O:36])[O:37][C:38]([CH3:39])([CH3:40])[CH3:41])[cH:42][cH:43]1.[CH3:137][CH2:138][O:139][C:140](=[O:141])[CH3:142].[CH3:143][O:144][CH2:145][CH2:146][O:147][CH3:148].[CH3:7][C:8]1([CH3:9])[C:10]([CH3:11])([CH3:12])[O:13][B:14]([c:15]2[c:16]([NH:21][C:22]([O:23][C:24]([CH3:25])([CH3:26])[CH3:27])=[O:28])[cH:17][cH:18][cH:19][cH:20]2)[O:29]1.[Na+:1].[Na+:2].[O-:3][C:4](=[O:5])[O-:6].[OH2:149].[OH:47][C:48]([CH2:49][C:50]([C:51](=[O:52])[OH:53])([CH2:54][C:55](=[O:56])[OH:57])[OH:58])=[O:59].[cH:60]1[cH:61][cH:62][c:63]([P:64]([Pd:65]([P:66]([c:67]2[cH:68][cH:69][cH:70][cH:71][cH:72]2)([c:73]2[cH:74][cH:75][cH:76][cH:77][cH:78]2)[c:79]2[cH:80][cH:81][cH:82][cH:83][cH:84]2)([P:85]([c:86]2[cH:87][cH:88][cH:89][cH:90][cH:91]2)([c:92]2[cH:93][cH:94][cH:95][cH:96][cH:97]2)[c:98]2[cH:99][cH:100][cH:101][cH:102][cH:103]2)[P:104]([c:105]2[cH:106][cH:107][cH:108][cH:109][cH:110]2)([c:111]2[cH:112][cH:113][cH:114][cH:115][cH:116]2)[c:117]2[cH:118][cH:119][cH:120][cH:121][cH:122]2)([c:123]2[cH:124][cH:125][cH:126][cH:127][cH:128]2)[c:129]2[cH:130][cH:131][cH:132][cH:133][cH:134]2)[cH:135][cH:136]1>>[c:15]1(-[c:31]2[cH:32][c:33]([N+:44](=[O:45])[O-:46])[c:34]([C:35](=[O:36])[O:37][C:38]([CH3:39])([CH3:40])[CH3:41])[cH:42][cH:43]2)[c:16]([NH:21][C:22]([O:23][C:24]([CH3:25])([CH3:26])[CH3:27])=[O:28])[cH:17][cH:18][cH:19][cH:20]1Participants
10
Reactant 9
Product 1
Sources & evidence
- ORD record
- ord-f3a2d1aadcae481b965006869d5c48b8
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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