HRID2134251

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

结构：C#[C][Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC

HCID621176

Tributylstannylacetylene

C14H28Sn

HCID59799911

2-(4-Bromo-2-methoxyphenyl)-5-methyl-1,3,4-oxadiazole

C10H9BrN2O2

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

HCID58063625

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-e197482485bd4043b2284a49075c363d
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (4/10)

反应 SMILES

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