Substructure Search

330340

CS(=O)(=O)Nc1cccc2c(C3(CCCI)CCc4cc(F)ccc43)c[nH]c12
Reaction #41996
title compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCCC1(c2c[nH]c3c(NS(C)(=O)=O)cccc23)CCc2cc(F)ccc21
Reaction #41997
title compound
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCN4CCOCC4)CCc4cc(F)ccc43)c[nH]c12
Reaction #41998
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c([C@H]2CC[C@@H](O)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45868
compound
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CCCC(C)C
Reaction #56727
2,2,6-Trimethyl-heptanoic acid methyl ester
Yield 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC(I)[N+](=O)[O-]
Reaction #61648
1-iodo-4-methyl-nitro-pentane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCn1c(=O)oc2ccccc21)[N+](=O)[O-]
Reaction #61649
oil
Yield 132.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCCI)[N+](=O)[O-]
Reaction #61663
1-iodo-4-methyl-4-nitro-pentane
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1[nH]c(=O)n2CCC(C)(C)[N+](=O)[O-]
Reaction #61668
4-methoxy-1-(3-methyl-3-nitro-butyl)-1,3-dihydro-benzimidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)n(C)c(=O)n2CCC(C)(C)[N+](=O)[O-]
Reaction #61670
5-methoxy-3-methyl-1-(3-methyl-3-nitro-butyl)-1,3-dihydro-benzimidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCC(C)(C)[N+](=O)[O-])c2cc(F)ccc21
Reaction #61672
5-fluoro-1-methyl-3-(4-methyl-4-nitro-pentyl)-1,3-dihydro-benzimidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COCC1CN(CCCC(c2ccc(F)cc2)c2ccc(F)cc2)CCN1C(=O)C(F)(F)F
Reaction #63599
4-[4,4-bis(4-fluorophenyl)butyl]-2-(methoxymethyl)-1-(trifluoroacetyl)piperazine
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63607
intermediate 94
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Cl)c1NC(=O)CN1CCN(CCCC(c2ccc(F)cc2)c2ccc(F)cc2)C(CO)C1
Reaction #63615
4-[4,4-bis(4-fluorophenyl)butyl]-N-(2-chloro-6-methylphenyl)-3-(hydroxymethyl)-1-piperazineacetamide
Yield 33.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Yield 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Yield 64.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81467
17-(3-Pyridyl)androsta-5,16-dien-3β-ol
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2CC1CCC2I
Reaction #84699
title compound
Yield 95.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC2OC2C1
Reaction #84700
compound
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@]2(Cc3ccccc3)CC[C@H](C(=O)N3CCN(c4ccccc4)CC3)[C@@H]1C2
Reaction #89769
crude product
DOI: 10.6084/m9.figshare.5104873.v1
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