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293707

CCCCCC1CCC(c2ccc(Br)c(C(=O)OC)c2F)CC1
Reaction #195219
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(c2ccc(C#C[Si](C)(C)C)cc2)CC1
Reaction #200156
DOI: 10.1039/C8SC04228D
CC1CC2C3CCC4=CC(=O)CCC4=C3C(c3ccc(-c4ncccn4)cc3)CC2(C)C1C(=O)C1CC1
Reaction #211200
DOI: 10.1039/C8SC04228D
CC1CC2C3CCC4=CC(=O)CCC4=C3C(c3ccc(Br)cc3)CC2(C)C1C(=O)C1CC1
Reaction #238089
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(c2ccc(-c3ccc(F)nc3F)cc2)CC1
Reaction #239554
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(c2ccc(-c3ccc(OCCCC)c(F)c3OCOCCOC)c(C(=O)OC)c2F)CC1
Reaction #240914
DOI: 10.1039/C8SC04228D
CC12CC(c3ccc(Br)cc3)C3=C4CCC(=O)CC4(O)CCC3C1CCC2C(=O)C1CC1
Reaction #266947
DOI: 10.1039/C8SC04228D
COc1ccc(-c2ccc(C3CC4(C)C(CC(C)C4C(=O)C4CC4)C4CCC5=CC(=O)CCC5=C34)cc2)cn1
Reaction #272161
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(c2ccc(C(=S)S)cc2)CC1
Reaction #386168
DOI: 10.1039/C8SC04228D
CCCCC[C@H]1CC[C@H](c2ccc(C#C[Si](C)(C)C)cc2)CC1
Reaction #486543
1-(trimethylsilylethynyl)-4-(trans-4-pentylcyclohexyl)benzene
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1CC[C@H](c2ccc(C(=S)S)cc2)CC1
Reaction #516891
4-(trans-4-n-pentylcyclohexyl)phenyldithiocarboxylic acid
Ausbeute 51.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1CC[C@H](c2ccc(C(=S)S)cc2)CC1
Reaction #722953
4-(trans-4-n-pentylcyclohexyl)phenyldithiocarboxylic acid
Ausbeute 51.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(-c4cccnc4)cc3)C[C@]2(C)[C@H]1C(=O)C1CC1
Reaction #725994
(11β,16α,17β)-17-cyclopropylcarbon-yl-16-methyl-11-[4-(3-pyridinyl)phenyl]estra-4,9-dien-3-one
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc([C@H]3C[C@@]4(C)[C@@H](C[C@@H](C)[C@@H]4C(=O)C4CC4)[C@@H]4CCC5=CC(=O)CCC5=C43)cc2)cn1
Reaction #725996
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(-c4ccc(F)nc4)cc3)C[C@]2(C)[C@H]1C(=O)C1CC1
Reaction #725997
product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cncc(-c2ccc([C@H]3C[C@@]4(C)[C@@H](C[C@@H](C)[C@@H]4C(=O)C4CC4)[C@@H]4CCC5=CC(=O)CCC5=C43)cc2)c1
Reaction #725998
product
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(-c4ccnnc4)cc3)C[C@]2(C)[C@H]1C(=O)C1CC1
Reaction #726000
(11β,16α,17β)-17-cyclopropylcarbonyl-16-methyl-11-[4-(4-pyridazinyl)phenyl]estra-4,9-dien-3-one
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(-c4cnccn4)cc3)C[C@]2(C)[C@H]1C(=O)C1CC1
Reaction #726001
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(-c4ccccn4)cc3)C[C@]2(C)[C@H]1C(=O)C1CC1
Reaction #726002
(11β,16α,17β)-17-cyclopropylcarbonyl-16-methyl-11-[4-(2-pyridinyl)phenyl]estra-4,9-dien-3-one
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(-c4ccncc4)cc3)C[C@]2(C)[C@H]1C(=O)C1CC1
Reaction #726003
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
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