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1317217

CC(C)(C)OC(=O)N1CCC(c2cnc(COc3ccc(S(C)(=O)=O)cc3)c(Cl)c2)CC1
Reaction #70447
title compound
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Cl)ccc(-c2cc(N)c(Cl)c(C(=O)NO)n2)c1F
Reaction #71524
powder
Rendimiento 103.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(OCC)c1ncc(C(=O)OCC)cc1Cl
Reaction #85728
ethyl 5-chloro-6-(1-ethoxyvinyl)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)cnc(CO)c1Cl
Reaction #168877
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)cnc(CCl)c1Cl.Cl
Reaction #168878
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(cc1Cl)CC1CN(C(=O)OC(C)(C)C)CC(C)N21
Reaction #175885
DOI: 10.1039/C8SC04228D
Nc1c(Cl)c(Oc2ccccc2)nc(C(=O)O)c1Cl
Reaction #211003
DOI: 10.1039/C8SC04228D
COC(=O)c1nc(C(C)=O)cc(Cl)c1Cl
Reaction #212429
DOI: 10.1039/C8SC04228D
CON=C(O)c1ncc(C(F)(F)F)cc1Cl
Reaction #226112
DOI: 10.1039/C8SC04228D
COC(=O)c1nc(-c2ccc(O)nc2)cc(N)c1Cl
Reaction #228393
DOI: 10.1039/C8SC04228D
COC(=O)c1nc(Br)cc([N+](=O)[O-])c1Cl
Reaction #228892
DOI: 10.1039/C8SC04228D
COC(=O)c1nc(-c2ccc(CF)cc2)cc(N)c1Cl
Reaction #230988
DOI: 10.1039/C8SC04228D
OCc1nc2c(cc1Cl)OCCN2
Reaction #231731
DOI: 10.1039/C8SC04228D
ClCc1nc(Cl)ccc1Cl
Reaction #232341
DOI: 10.1039/C8SC04228D
OC(c1ccncc1)c1nc(Cl)ccc1Cl
Reaction #234835
DOI: 10.1039/C8SC04228D
CCC(Nc1ccnc(COC)c1Cl)c1ccc(OC(F)F)cc1
Reaction #239732
DOI: 10.1039/C8SC04228D
CCOC(=O)c1nc2ccccc2c(OCc2ccccc2)c1Cl
Reaction #241553
DOI: 10.1039/C8SC04228D
COC1(c2ncccc2Cl)CCC(=O)CC1
Reaction #247027
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(OCc2nc(Cl)ccc2Cl)cc1
Reaction #254315
DOI: 10.1039/C8SC04228D
COc1ccc(Cl)c(C(=O)O)n1
Reaction #258760
DOI: 10.1039/C8SC04228D
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