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NCc1cccc(O)c1

COc1cccc(C(=O)N(CCO)c2ccccc2OC)c1
Reaction #2559
title compound
المردود 86.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(=O)N(CC=O)c2ccccc2OC)c1
Reaction #2560
title compound
المردود 65.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(CC(=O)O)N2C(=O)c3ccccc3C2=O)cc1OC1CCCC1
Reaction #9925
3-(3-cyclopentyloxy-4-methoxy-phenyl)-3-phthalimidopropanoic acid
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #10417
ethyl acetate hexanes
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CNC[C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)c1.O=C(O)C(F)(F)F
Reaction #42285
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42286
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(N)=O)cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42292
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)c1cc(C(=O)N(CCC)[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)cc(S(N)(=O)=O)c1
Reaction #42294
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CC)cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42295
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)N(CCC)c1cc(C)cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CC#N)cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42303
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CO)cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42304
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(C(F)(F)F)c2)cc(C(=O)N(CCC)CCC)c1
Reaction #42307
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)cc(-c2ccc(OC)cc2)c1.Cl
Reaction #42310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(OC)c2)cc(-c2ccccc2)c1.Cl
Reaction #42311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(OC)c2)cc(-c2ccsc2)c1.Cl
Reaction #42315
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)c1cc(C)cc(C(=O)N[C@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42317
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2ccc(OCc3ccccc3)cc2)[C@H](O)CNCc2cccc(OC)c2)c1
Reaction #42324
N1-{(1S,2R)-1-[4-(benzyloxy)benzyl]-2-hydroxy-3-[(3-methoxybenzyl)amino]propyl}-5-methyl-N3,N3-dipropylisophthalamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCCCc2ccc(C)cc2C)c1
Reaction #42326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)NCCCOc1cc(I)c2c(c1Cl)CNC2=O
Reaction #49607
4-chloro-5-[3-(ethylcarbamoylamino)propoxy]-7-iodoisoindolinone
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
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