1-bromo-4-phenylmethoxybenzene

C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #202
Выход 35.7%750 AstraZeneca ELN dataset
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #203
Выход 0.0%750 AstraZeneca ELN dataset
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #204
Выход 31.5%750 AstraZeneca ELN dataset
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #205
Выход 0.0%750 AstraZeneca ELN dataset
C[C@H](CNc1ccc(OCc2ccccc2)cc1)O[Si](C)(C)C(C)(C)C
Reaction #434
Выход 65.2%750 AstraZeneca ELN dataset
C[C@H](CNc1ccc(OCc2ccccc2)cc1)O[Si](C)(C)C(C)(C)C
Reaction #435
Выход 18.9%750 AstraZeneca ELN dataset
O=C1CN(c2ccncc2)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #2348
4-benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene
Выход 123.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC1(c2ccc(OCc3ccccc3)cc2)CCOCC1
Reaction #79367
4-(4-benzyloxyphenyl)tetrahydro-2H-pyran-4-ol
Выход 55.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C1Nc2ccccc2C1=O
Reaction #191738
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(c1ccccc1)N1CCC(O)(c2ccc(OCc3ccccc3)cc2)CC1
Reaction #200690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(CCC(=O)c1ccc(OCc2ccccc2)cc1)NC(=O)OC(C)(C)C
Reaction #229138
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC1(c2ccc(OCc3ccccc3)cc2)CCC2(CC1)OCCO2
Reaction #275040
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(C)(C)C(=O)c1ccc(OCc2ccccc2)cc1
Reaction #295430
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)CCC(O)(c2ccc(OCc3ccccc3)cc2)CC1
Reaction #324917
1-(4-benzyloxy-phenyl)-4,4-dimethylcyclohexanol
Выход 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC1(C)CCCC(O)(c2ccc(OCc3ccccc3)cc2)C1
Reaction #324940
1-(4-benzyloxy-phenyl)-3,3-dimethyl-cyclohexanol
Выход 53.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C1CN(c2ccncc2)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #353951
4-benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene
Выход 123.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
FC(F)(F)Oc1ccc(OC2CCN(c3ccc(OCc4ccccc4)cc3)CC2)cc1
Reaction #380514
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
c1ccc(COc2ccc(-n3ccc4c(OCc5ccccc5)cccc43)cc2)cc1
Reaction #407575
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC(C)(C)C(=O)C(=O)N1CCCC1C(=O)CCC=Cc1ccc(OCc2ccccc2)cc1
Reaction #411759
3,3-dimethyl-1-(2-{5-[4-(phenylmethoxy)phenyl]pent-4-enoyl}pyrrolidinyl)pentane-1,2-dione
Выход 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Nc1ccccc1C(=O)c1ccc(OCc2ccccc2)cc1
Reaction #432016
4'-benzyloxy-2-aminobenzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
Страница 1Далее