HRID143923

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8071

未命名化合物

HCID689082

2-chloro-8-methylquinoline-3-carbaldehyde

C11H8ClNO

结构：CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ncco1

HCID15486183

2-(Tributylstannyl)-1,3-oxazole

C15H29NOSn

结构：c1ccc([PH](c2ccccc2)(c2ccccc2)[Pd]([PH](c2ccccc2)(c2ccccc2)c2ccccc2)([PH](c2ccccc2)(c2ccccc2)c2ccccc2)[PH](c2ccccc2)(c2ccccc2)c2ccccc2)cc1

HCID178420554

未命名化合物

PRODUCTS

生成物

HCID86653032

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-4297cd87de8d4e9e8a5b0030723a7f24
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (9/10)

反应 SMILES

[CH2:15]([Sn:16]([CH2:17][CH2:18][CH2:19][CH3:25])([c:20]1[o:21][cH:22][cH:23][n:24]1)[CH2:26][CH2:27][CH2:28][CH3:29])[CH2:30][CH2:31][CH3:32].[CH3:33][O:34][CH2:35][CH2:36][O:37][CH3:38].[Cl:1][c:2]1[n:3][c:4]2[c:5]([CH3:14])[cH:6][cH:7][cH:8][c:9]2[cH:10][c:11]1[CH:12]=[O:13].[cH:39]1[cH:40][cH:41][c:42]([P:43]([Pd:44]([P:45]([c:46]2[cH:47][cH:48][cH:49][cH:50][cH:51]2)([c:52]2[cH:53][cH:54][cH:55][cH:56][cH:57]2)[c:58]2[cH:59][cH:60][cH:61][cH:62][cH:63]2)([P:64]([c:65]2[cH:66][cH:67][cH:68][cH:69][cH:70]2)([c:71]2[cH:72][cH:73][cH:74][cH:75][cH:76]2)[c:77]2[cH:78][cH:79][cH:80][cH:81][cH:82]2)[P:83]([c:84]2[cH:85][cH:86][cH:87][cH:88][cH:89]2)([c:90]2[cH:91][cH:92][cH:93][cH:94][cH:95]2)[c:96]2[cH:97][cH:98][cH:99][cH:100][cH:101]2)([c:102]2[cH:103][cH:104][cH:105][cH:106][cH:107]2)[c:108]2[cH:109][cH:110][cH:111][cH:112][cH:113]2)[cH:114][cH:115]1>>[c:2]1(-[c:20]2[o:21][cH:22][cH:23][n:24]2)[n:3][c:4]2[c:5]([CH3:14])[cH:6][cH:7][cH:8][c:9]2[cH:10][c:11]1[CH:12]=[O:13]