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CCCCN1CCC(CC2CCCC3c4ccccc4N(C(=O)O)C23)CC1
Reaction #1712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCC(Cc2cccc3c4ccccc4n(C(=O)O)c23)CC1
Reaction #1713
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)O)NC1=O
Reaction #5491
trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)OCCCc1ccncc1
Reaction #11562
titled compound
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C[C@@H](CCC1CCCCC1)C(=O)N1C(=O)OC[C@@H]1Cc1ccccc1
Reaction #43555
3-(R)-(4-(S)-Benzyl-2-oxo-oxazolidine-3-carbonyl)-5-cyclohexyl-pentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[C@@H](CCC1CCCCC1)C(=O)N1C(=O)OC[C@@H]1Cc1ccccc1)N1CCOCC1
Reaction #43556
1-(4-(S)-Benzyl-2-oxo-oxazolidin-3-yl)-2-(R)-(2-cyclohexyl-ethyl)-4-morpholin-4-yl-butane-1,4-dione
Rendimiento 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)OCCCc1ccncc1
Reaction #46681
compound
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48643
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](CCC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48644
title compound
Rendimiento 37.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)O)NC1=O
Reaction #50245
trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCC[C@H]1CC[C@H](N(C)C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #53902
trans-{4-[4-(Allyl-methyl-amino)-butyl]-cyclohexyl}-methyl-carbamic acid 4-chloro-phenyl ester
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(=O)NN
Reaction #78019
decanoic acid hydrazide
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)[C@@H]1C[C@H]1c1ccc([N+](=O)[O-])cc1
Reaction #95094
trans-N-(1-Methyldecyl)-2-(4-nitrophenyl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)[C@@H]1C[C@H]1c1ccc(N)cc1
Reaction #95097
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCCCCCCCCCCCCO
Reaction #162013
12-Azido-1-dodecanol
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)Cn3ccc4ccccc43)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172765
title compound
Rendimiento 31.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)CN3CCN(C(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172767
title compound
Rendimiento 22.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)C3CCCN3S(C)(=O)=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172776
title compound
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)CN3CCC(F)(F)C3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172779
title compound
Rendimiento 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(F)(F)F
Reaction #172788
TFA
Rendimiento 54.1%DOI: 10.6084/m9.figshare.5104873.v1
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