Recherche de Sous-structure

1159654

CC(CC(=O)O)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55195
3-(2',4'-difluoro-4-biphenylyl)butyric acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93229
dihydrobenzothiophenes
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](OC5CCCOC5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #95326
(24R)-5,7-cholestadiene-3β,24,25-triol 3-tetrahydropyranyl ether
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1c2ccccc2CCc2cc(Cl)ccc21
Reaction #95918
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #316508
Sulfone
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@H](OCc2ccccc2)C[C@H](CCc2ccc(Cl)cc2Cl)O1
Reaction #412724
title compound
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCC(C)CCCC(C)CCCC(C)CCOc1ccc(C(=O)O)s1
Reaction #415561
5-(3,7,11,15-Tetramethylhexadecyloxy)-2-thiophenecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(Cc2ccc(C(O)CCc3ccccc3)nc2)S1
Reaction #433382
desired product
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #486267
N-carbo-(-)-menthyloxy pyrrole
DOI: 10.6084/m9.figshare.5104873.v1
NC1=Nc2ccc(Cl)cc2C(c2ccc(N)cc2)C1
Reaction #512442
2-Amino-4-(4-aminophenyl)-6-chloro-3,4-dihydroquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(CC(=O)O)C(C)(C)CC1
Reaction #572220
3,3,6,6-tetramethyl-1-cyclohexen-1-acetic acid
Rendement 84.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(CCOc2cc(C(=O)NC3(C(=O)O)Cc4ccccc4C3)ccc2OC2CC2)c1
Reaction #608708
2-[4-Cyclopropoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(CC(=O)O)C(C)(C)CC1
Reaction #630089
3,3,6,6-tetramethyl-1-cyclohexen-1-acetic acid
Rendement 84.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCC(C)CCCC(C)CCCC(C)CCOc1ccc(C(=O)O)s1
Reaction #683841
5-(3,7,11,15-Tetramethylhexadecyloxy)-2-thiophenecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1Cc2cc(F)ccc2O1
Reaction #735402
5-Fluoro-2,3-dihydrobenzofuran-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCCOc1ccc(O)cc1
Reaction #950544
p-(10-undecenyl)oxyphenol
Rendement 47.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(Cc2ccc(C(O)CCc3ccccc3)nc2)S1
Reaction #980004
desired product
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)Oc1ccc(OC2CC2)c([C@H]2CO[C@]3(CC[C@@H]4CC[C@]3(c3ccccc3)N4)C2)c1
Reaction #1104465
title compound
Rendement 61.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc(OC(F)(F)F)cc([C@H]3CO[C@]4(CC[C@@H]5CC[C@]4(c4ccccc4)N5)C3)c2O1
Reaction #1104467
title compound
Rendement 69.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(OC2CC2)cn1
Reaction #1125760
title compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
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