Участвует в 39 реакциях

5717

O=C(O)C1CCc2ccccc2C1
Reaction #1509
1,2,3,4-tetrahydro-2-naphthalenecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1nn2c(-c3c(C)cc(C)cc3OC)ccc(OC)c2c1[N+](=O)[O-]
Reaction #9287
title compound
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1csc(-c2ccccc2Cl)n1
Reaction #228349
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C(=O)C(=O)c2ccc(C#N)c(-c3cccnc3)c2)cc1C
Reaction #235580
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=Cc1cc(O)cc2nc(-c3ccc(O)c(F)c3)oc12
Reaction #258005
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(Oc2ccc(C3(Cn4cncn4)OCCO3)cc2)cc1
Reaction #345521
2-[p-(Phenoxy)-phenyl]-2-[1-(1H-1,2,4-triazolyl)-methyl]-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
Cc1cc(N2CCOCC2)c(Cl)cc1[N+](=O)[O-]
Reaction #397552
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(O)CN1c2ccccc2N(CC(C)O)c2ccccc21
Reaction #500792
5,10-bis(2-Hydroxypropyl)-5,10-dihydrophenazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
C=Cc1cc(O)cc2nc(-c3ccc(O)c(F)c3)oc12
Reaction #578916
solid
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(O)CC=CC1CCN(C(=O)OCc2ccccc2)CC1
Reaction #655300
3-(1-phenylmethoxycarbonyl-4-piperidinylmethylene)propanoic acid
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
COc1ccc(C(=O)C(=O)c2ccc(C#N)c(-c3cccnc3)c2)cc1C
Reaction #730657
title compound
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CN1CC(c2ccc(Nc3cc(Br)cn(C)c3=O)nc2)C1
Reaction #785257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)C=Cc1ccc(OC)c(F)c1
Reaction #785562
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCc1nn2c(-c3c(C)cc(C)cc3OC)ccc(OC)c2c1[N+](=O)[O-]
Reaction #904087
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
C=Cc1cc(O)cc2nc(-c3ccc(O)c(F)c3)oc12
Reaction #945421
solid
Выход 72.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_12
F.O=[N+]([O-])c1ccc(N2CCN3CCC2CC3)cc1
Reaction #969905
4-(4-Nitro-phenyl)-1,4-diaza-bicyclo[3.2.2]nonane hydrofluoric acid salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCOC(=O)C=Cc1ccc(OC)c(F)c1
Reaction #1071883
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
C=Cc1cc(O)cc2nc(-c3ccc(O)c(F)c3)oc12
Reaction #1094529
solid
Выход 72.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
COc1ccc(CN2CCN(CCC(c3ccccc3)c3ccccc3)CC2)c(OC)c1OC
Reaction #1163967
1-(3,3-diphenylpropyl)-4-(2,3,4-trimethoxybenzyl)piperazine
Выход 91.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_05
O=C(O)CC=CC1CCN(C(=O)OCc2ccccc2)CC1
Reaction #1211467
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
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