HRID298539

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID8857

Ethyl acetate

C4H8O2

HCID11776

Triphenylphosphine

C18H15P

HCID220568

Diethyl azodicarboxylate

C6H10N2O4

HCID2794620

benzyl 4-hydroxypiperidine-1-carboxylate

C13H17NO3

结构：COC(=O)C(Cc1ccc(O)cc1)NC(=O)OC(C)(C)C

HCID4459028

Methyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}tyrosinate

C15H21NO5

PRODUCTS

生成物

结构：COC(=O)C(Cc1ccc(OC2CCN(C(=O)OCc3ccccc3)CC2)cc1)NC(=O)OC(C)(C)C

HCID178499943

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-4d11b02f59a142c08a1db50ff345eaa5
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (8/10)

反应 SMILES

[C:18]([CH3:19])([CH3:20])([CH3:21])[O:22][C:23](=[O:24])[NH:25][CH:26]([C:27](=[O:28])[O:29][CH3:30])[CH2:31][c:32]1[cH:33][cH:34][c:35]([OH:38])[cH:36][cH:37]1.[CH3:75][CH2:76][O:77][C:78](=[O:79])[CH3:80].[O:58]=[C:59]([O:60][CH2:61][CH3:62])[N:63]=[N:64][C:65]([O:66][CH2:67][CH3:68])=[O:69].[O:70]1[CH2:71][CH2:72][CH2:73][CH2:74]1.[OH:1][CH:2]1[CH2:3][CH2:4][N:5]([C:8](=[O:9])[O:10][CH2:11][c:12]2[cH:13][cH:14][cH:15][cH:16][cH:17]2)[CH2:6][CH2:7]1.[c:39]1([P:40]([c:41]2[cH:42][cH:43][cH:44][cH:45][cH:46]2)[c:47]2[cH:48][cH:49][cH:50][cH:51][cH:52]2)[cH:53][cH:54][cH:55][cH:56][cH:57]1>>[O:1]([CH:2]1[CH2:3][CH2:4][N:5]([C:8](=[O:9])[O:10][CH2:11][c:12]2[cH:13][cH:14][cH:15][cH:16][cH:17]2)[CH2:6][CH2:7]1)[c:35]1[cH:34][cH:33][c:32]([CH2:31][CH:26]([NH:25][C:23]([O:22][C:18]([CH3:19])([CH3:20])[CH3:21])=[O:24])[C:27](=[O:28])[O:29][CH3:30])[cH:37][cH:36]1