anisole

COC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccccc1
Reaction #98
Ausbeute 57.5%750 AstraZeneca ELN dataset
COC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccccc1
Reaction #99
Ausbeute 65.4%750 AstraZeneca ELN dataset
COC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccccc1
Reaction #100
Ausbeute 75.1%750 AstraZeneca ELN dataset
COc1cc(N2CCN(C(C)=O)CC2)ccc1Nc1ncc(Cl)c(-c2cnc3cc(N4CCCC4)ccn23)n1
Reaction #210
Ausbeute 0.0%750 AstraZeneca ELN dataset
CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #441
Ausbeute 0.0%750 AstraZeneca ELN dataset
CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #442
Ausbeute 0.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #453
Ausbeute 49.6%750 AstraZeneca ELN dataset
COc1cccc(Nc2cccc(C(F)(F)F)c2)c1
Reaction #756
Ausbeute 0.0%750 AstraZeneca ELN dataset
CC1(N)CCN(c2nccc(Cl)n2)CC1
Reaction #1252
4-amino-1-(4-chloropyrimidin-2-yl)-4-methylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(N)CCN(c2ccnc(Cl)n2)CC1
Reaction #1253
4-amino-1-(2-chloropyrimidin-4-yl)-4-methylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N[C@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)OCc1ccccc1.O=C(O)C(F)(F)F
Reaction #1683
white powder
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@H](N)CCc1ccccc1
Reaction #2010
D-Homophenylalanine allyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(OCC(=O)O)cc2)cc1
Reaction #2384
4-{2-[6-(4-tert-butylbenzenesulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yl-oxy]ethoxy}phenoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CC(C(=O)O)N1Cc2ccccc2CC(NC(=O)C(Cc2ccccc2)SC(=O)c2ccccc2)C1=O
Reaction #2812
title compound
Ausbeute 122.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3025
2,5-dichlorobenzophenones
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C(=O)NC(CC(C)C)C(=O)O)c(SSc2cc(OC)ccc2C(=O)NC(CC(C)C)C(=O)O)c1
Reaction #3349
title compound
Ausbeute 69.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CC(NC(=O)c1cc(F)ccc1SSc1ccc(F)cc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3350
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cccc([SH](Sc2cc(C)ccc2C(=O)NC(CC(C)C)C(=O)O)C(=O)NC(CC(C)C)C(=O)O)c1
Reaction #3351
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CC(NC(=O)c1cccnc1SSc1ncccc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3352
title compound
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)C1=C(CCl)CS[C@@H]2[C@H](NC(=S)Cc3cc(Cl)ccc3Cl)C(=O)N12
Reaction #3761
(6R)-trans-3-chloromethyl-7-[(2,5-dichlorophenyl)-thioacetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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