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CCc1ccc(I)cc1

N#Cc1ccc([C@@]2(O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1Cc1ccc(C(F)(F)C(F)(F)F)cc1
Reaction #48115
4-(β-D-glucopyranos-1-yl)-2-(4-pentafluoroethyl-benzyl)-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4cc(I)c(O)cc4C[C@H](O)[C@H]3[C@@H]1CCC2=O
Reaction #56618
colorless crystals
Ausbeute 68.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1Cc2cc(O)c(I)cc2[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12
Reaction #56619
7β-Acetoxy-3-hydroxy-2-iodo-estra-1,3,5(10)-trien-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[N+](C)(C)CCOP(=O)([O-])OCCCCCCCCCCCCCCCCCCc1ccc([131I])cc1
Reaction #72397
131I-NM404
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)c2cc(I)ccc21
Reaction #81550
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ncn(-c3ccc(C(F)(F)C(F)(F)C(F)(F)F)cc3)n2)cc1
Reaction #88154
1-(4-(perfluoropropyl)phenyl)-3-(p-tolyl)-1H-1,2,4-triazole
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1I)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #90155
title compound
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1N1CCC(O)CC1)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #90158
9-Ethyl-8-(4-hydroxy-piperidin-1-yl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(I)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #159447
3-(2-ethyl-5-iodophenyl)bicyclo[3.2.1]-octane-2,4-dione
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(B(O)O)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #159448
3-(2,4-dioxo-bicyclo[3.2.1]oct-3-yl)-4-ethylphenylboronic acid
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCc1ccc(I)cc1
Reaction #163339
N-(4-iodophenethyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(C)CCc2ccc(Cl)cc21
Reaction #171248
N-methyl-8-Chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1Br)C(C)CNCC2
Reaction #171249
8-Bromo-7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1I)C(C)CNCC2
Reaction #171258
yellow solid
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1CNCCc2cc(O)c(I)cc21
Reaction #171270
white solid
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1cc2c(cc1I)C(C)CNCC2
Reaction #171272
white solid
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC1(c2ccc(I)cc2)CCN(CC2CC2)CC1)C(=O)Nc1cc(Cl)cc(Cl)c1
Reaction #174975
DOI: 10.1039/C8SC04228D
CCC(Cc1c(I)cc(I)c(NC(=O)CCl)c1I)C(=O)O
Reaction #177229
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(I)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #182436
DOI: 10.1039/C8SC04228D
C=C(c1ccc(NC=O)cc1)C(O)(Cn1cncn1)c1ccc(F)cc1F
Reaction #198146
DOI: 10.1039/C8SC04228D
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