4-cyano-4′-hydroxybiphenyl

COCOc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #192509
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1(COc2ccc(-c3ccc(C#N)cc3)cc2)CCN(C(=O)c2ccc(OC)cc2)C1
Reaction #196627
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #211430
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1(COc2ccc(-c3ccc(C#N)cc3)cc2)CCN(C(=O)c2ccccc2OC)C1
Reaction #235120
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(-c2ccc(CCCO)cc2)cc1
Reaction #236826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(-c2ccc(OCCCCCCCCO)cc2)cc1
Reaction #237224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)COc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #246726
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCOC(=O)Oc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #262308
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)c1ccc(-c2ccc(O)cc2)cc1
Reaction #321737
4'-Hydroxybiphenyl-4-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(C)(C)OC(=O)COc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #322162
4-(tert.Butyloxycarbonylmethyloxy)-4'-cyano-biphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
C=CCOc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #344474
white crystalline material
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
N#Cc1ccc(-c2ccc(OCCCCCCBr)cc2)cc1
Reaction #361332
4'-(6-bromohexyloxy)-4-cyanobiphenyl
المردود 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
N#Cc1ccc(-c2ccc(OCCCCBr)cc2)cc1
Reaction #361333
4'-(4-bromobutyloxy)-4-cyanobiphenyl
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
N#Cc1ccc(-c2ccc(OCCCCCCO)cc2)cc1
Reaction #361334
4'-(6-hydroxyhexyloxy)-4-cyanobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
N#Cc1ccc(-c2ccc(OCCCO)cc2)cc1
Reaction #384082
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCCCCOC(=O)Oc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #384393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#Cc1ccc(-c2ccc(OCCCO)cc2)cc1
Reaction #430819
4-cyano-4'-(3-hydroxypropoxy)biphenyl
المردود 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
N#Cc1ccc(-c2ccc(OCCCCCCO)cc2)cc1
Reaction #430823
4-cyano-4'-(6-hydroxyhexyloxy)biphenyl
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(C)N(C(=O)COc1ccc(-c2ccc(C#N)cc2)cc1)C(C)C
Reaction #487438
expected product
المردود 89.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCCCCCCCCCOc1ccc(-c2ccc(C#N)cc2)cc1
Reaction #529770
4-Cyano-4'-decyloxybiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
الصفحة 1التالي