Busqueda de Similitud

Cl.NCCC(N)=O

NC(=O)CCNc1ccc(C(=O)O)cc1
Reaction #686
Rendimiento 0.0%
CCOC(=O)CCNc1c2ccc(Cl)cc2nc2c(=O)[nH][nH]c(=O)c12
Reaction #3235
ester
Rendimiento 13.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11725
title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11732
title compound
Rendimiento 38.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)OCc1ccccc1
Reaction #45704
Ethyl 3-(benzyloxycarbonylamino)propionate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC1CCN(C(=O)OCc2ccccc2)CC1
Reaction #48519
title compound
Rendimiento 87.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(Cc2ccc(-c3cncnc3)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCCC(N)=O)n21
Reaction #52121
title compound
Rendimiento 10.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC(=O)N1CCCC2CCCCC21
Reaction #67494
intermediate
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC(=O)c1ccc(CN(C(=O)N[C@@H](C)c2ccc(Cl)cc2)c2ccc(C3CCCCC3)cc2)cc1
Reaction #77825
3-{4-[3-[1(S)-(4-chloro-phenyl)ethyl]1-(4-cyclohexylphenyl)ureidomethyl]benzoylamino}propionic acid methyl ester
Rendimiento 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNCC(N)=O
Reaction #79462
title compound
Rendimiento 51.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)c1ccn(CC)c1
Reaction #79512
Ethyl 3-(1-ethyl-3-pyrrolecarboxamido)propionate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)c1c[nH]cc1C
Reaction #79513
title compound
Rendimiento 43.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNc1nc(Cl)cc2nccnc12
Reaction #85903
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC(=O)N1CCCC2CCCCC21
Reaction #155511
intermediate
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC(=O)[C@@H](CC(=O)OC(C)(C)C)Cc1ccc(-c2ccccc2)cc1
Reaction #158046
(R)-tert-butyl 3-(biphenyl-4-ylmethyl)-4-(3-methoxy-3-oxopropylamino)-4-oxobutanoate
Rendimiento 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)CC1CCC(c2ccc(-c3cnc(Nc4cccc(Cl)c4)o3)cc2)CC1
Reaction #163221
title compound
Rendimiento 113.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC(=O)CCC1CCSS1
Reaction #179429
DOI: 10.1039/C8SC04228D
CCOC(=O)CCNC(=O)CCC(=O)Nc1ccc(C=NN)cc1
Reaction #180541
DOI: 10.1039/C8SC04228D
CCOC(=O)CCNC(=O)c1ccc(NC(CCCCOC)c2oc3ccc(OC)cc3c2C)cc1
Reaction #183196
DOI: 10.1039/C8SC04228D
CCOC(=O)CCN1C(=O)c2ccc(C)cc2C1=O
Reaction #185021
DOI: 10.1039/C8SC04228D
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