Recherche de Sous-structure

NC=O

COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1294
title product
Rendement 196.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1430
title product
Rendement 196.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2C(F)(F)F)cc1
Reaction #2581
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1)c1ccccc1
Reaction #2615
title compound
Rendement 71.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1C(=O)c2ccccc2C1=O)C(C)=O
Reaction #10933
desired product
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCCCCCNC(=O)C(F)(F)F
Reaction #11999
amide
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C1Cc1n[nH]c(=S)[nH]c1=O
Reaction #46259
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #54591
ethyl α-phthalimidopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCNC(=O)OC(C)(C)C)OP(=O)(OC)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #58021
2-[(1-benzyloxycarbonylamino-2-methyl-propyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCc1c(OC)cccc1C(=O)NN(C(=O)c1cc(C)cc(C)c1)C(C)(C)C
Reaction #67913
3,5-dimethyl-benzoic acid N′-(2-allyloxymethyl-3-methoxy-benzoyl)-N-tert-butyl-hydrazide
Rendement 83.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(COCCP(=O)(O)O)C(=O)N(CC)CC
Reaction #78328
bight yellow oil
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCCCCCNC(=O)C(F)(F)F
Reaction #88689
amide
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(CN2C(=O)c3ccccc3C2=O)cc1O
Reaction #157287
product
Rendement 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)c1[nH]c2ccc(Br)cc2c1CC(=O)O
Reaction #177995
DOI: 10.1039/C8SC04228D
CC(NC(=O)Cc1cc(F)cc(F)c1)C(=O)NC(C)C(=O)N1CCSC1
Reaction #181905
DOI: 10.1039/C8SC04228D
Cc1cc(C(O)(C(F)(F)F)C(F)(F)F)cc(C)c1NC(=O)c1cccc(NC(=O)c2ccccc2)c1
Reaction #185800
DOI: 10.1039/C8SC04228D
COC(=O)CCC(=O)c1ccc2c(c1)CC(CNC(C)=O)C2
Reaction #187326
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCN(C(=O)C5CC5)CC4)[nH]c3cc2Br)CC1
Reaction #188624
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(-c2ccccc2)ccc1O)c1ccc(C(C(=O)Nc2ccccc2)C(=O)Nc2ccccc2)cc1
Reaction #189628
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3n2C(C)C)CC1
Reaction #190962
DOI: 10.1039/C8SC04228D
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