HRID583621

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID3672

Ibuprofen

C13H18O2

HCID95631

2-(Acetylamino)-3-phenyl-2-propenoic acid

C11H11NO3

结构：O=S(=O)([O-])c1ccc(CCCc2ccc(P(c3ccc(CCCc4ccc(S(=O)(=O)[O-])cc4)cc3)c3ccc4ccccc4c3-c3c(P(c4ccc(CCCc5ccc(S(=O)(=O)[O-])cc5)cc4)c4ccc(CCCc5ccc(S(=O)(=O)[O-])cc5)cc4)ccc4ccccc34)cc2)cc1

HCID19347541

未命名化合物

PRODUCTS

生成物

结构：c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1

HCID634876

2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl

C44H32P2

PROCEDURE

实验过程

According to Example 6, 2-(4-isobutylphenyl) propanoic acid and the methyl ester of acetylaminocinnamic acid were asymmetrically hydrogenated with the Rh- or Ru complexes of (R)-(+)-BINAP-C3 -TS (Table 4).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d969d650eda74cc1b8497eaf1c7c5c94
来源数据集: uspto-grants-1999_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05929273
来源说明: uspto-grants-1999_07

反应 SMILES

C(C1C=CC(C(C)C(O)=O)=CC=1)C(C)C.C(NC(=CC1C=CC=CC=1)C(O)=O)(=O)C.S(C1C=CC(CCC[C:44]2[CH:49]=[CH:48][C:47]([P:50]([C:110]3[CH:115]=[CH:114][C:113](CCCC4C=CC(S([O-])(=O)=O)=CC=4)=[CH:112][CH:111]=3)[C:51]3[CH:60]=[CH:59][C:58]4[C:53](=[CH:54][CH:55]=[CH:56][CH:57]=4)[C:52]=3[C:61]3[C:70]4[C:65](=[CH:66][CH:67]=[CH:68][CH:69]=4)[CH:64]=[CH:63][C:62]=3[P:71]([C:91]3[CH:96]=[CH:95][C:94](CCCC4C=CC(S([O-])(=O)=O)=CC=4)=[CH:93][CH:92]=3)[C:72]3[CH:77]=[CH:76][C:75](CCCC4C=CC(S([O-])(=O)=O)=CC=4)=[CH:74][CH:73]=3)=[CH:46][CH:45]=2)=CC=1)([O-])(=O)=O>>[CH:113]1[CH:112]=[CH:111][C:110]([P:50]([C:51]2[CH:60]=[CH:59][C:58]3[C:53](=[CH:54][CH:55]=[CH:56][CH:57]=3)[C:52]=2[C:61]2[C:70]3[C:65](=[CH:66][CH:67]=[CH:68][CH:69]=3)[CH:64]=[CH:63][C:62]=2[P:71]([C:72]2[CH:77]=[CH:76][CH:75]=[CH:74][CH:73]=2)[C:91]2[CH:96]=[CH:95][CH:94]=[CH:93][CH:92]=2)[C:47]2[CH:46]=[CH:45][CH:44]=[CH:49][CH:48]=2)=[CH:115][CH:114]=1