carbonate

Cc1nc2c(OCC3CCCCC3)cccn2c1C(=O)NC1CC1
Reaction #92756
8-(cyclohexylmethoxy)-N-cyclopropyl-2-methylimidazo[1,2-a]pyridine-3-carboxamide
Выход 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nc2c(OCC3CCCCC3)cccn2c1C(=O)N[C@H](C(=O)O)c1ccccc1
Reaction #92757
(2S)-({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)(phenyl)acetic acid
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nc2c(OCC3CCCCC3)cccn2c1C(=O)N[C@@H](CC(=O)O)Cc1ccccc1
Reaction #92758
(3R)-3-({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)-4-phenylbutanoic acid
Выход 61.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOP(=O)(OCC)Oc1cc2c(c3ccccc13)Nc1ccccc1S2
Reaction #93248
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC(C)C(=O)Nc1c[nH]c2ncc(Br)nc12
Reaction #155844
N-(2-bromo-5H-pyrrolo[2,3-b]pyrazin-7-yl)isobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc2[nH]c(=O)c3cnn(C4CCOCC4)c3c2cc1C(=O)N1CCC(c2cccc(C(=O)O)c2)CC1
Reaction #156316
3-(1-{[7-methyl-4-oxo-1-(tetrahydro-2H-pyran-4-yl)-4,5-dihydro-1H-pyrazolo[4,3-c]quinolin-8-yl]carbonyl}piperidin-4-yl)benzoic acid
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(CBr)C(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)COP(=O)(O)O
Reaction #164456
Bromoacetyl Glucose-6-Phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCSCCCNC(=O)OC(C)(C)C
Reaction #172999
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(CC)(c1ccc(O)c(C)c1)c1ccc(-c2sc(C(=O)OC)cc2C)c(C)c1
Reaction #173018
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cccnc1SCCSc1ccccc1
Reaction #173019
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCC(=NO)c1ccc(-c2ccc(Cl)cc2F)cc1
Reaction #173040
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOc1ccc(O)cc1
Reaction #173074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc([N+](=O)[O-])cnc1Oc1ccc(Cl)c(C(F)(F)F)c1
Reaction #173078
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(SCCCSc2sccc2[N+](=O)[O-])ccnc1CO
Reaction #173086
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C=O)C1CCC2C(O)CCCC12C
Reaction #173090
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1cc(OCCCNC2Cc3ccccc3C2)cc(-c2noc3ccsc23)c1
Reaction #173093
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1c(-c2ccccc2)nc(CN2CCN(c3ccc(O)cc3)CC2)cc1=O
Reaction #173096
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN1c2ccc(F)c(N)c2CS1(=O)=O
Reaction #173104
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1c(S(=O)c2ccccc2-c2ccccn2)nc2ccccc21
Reaction #173107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C(=O)NC2CC2)cc1-c1ccc2c(=O)n(C(C)c3ccccc3)ccc2c1
Reaction #173109
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
НазадСтраница 2Далее