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16760005

CCCC[C@@H](C)C[C@@H](/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)C(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3123
methyl(11R,12S,13E,15S,17R)-9-isobutyryloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(C(=O)N(CCCCN3CCN(c4ncccn4)CC3)C1=O)C2(C)C
Reaction #5013
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(C)(C1)C(=O)N(CCCCN1CCN(c3ncccn3)CC1)C2=O
Reaction #5017
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCC(CC2)C(=O)N1CCCCN1CCN(c2ncccn2)CC1
Reaction #5018
title compound
Ausbeute 8.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2CCC1CC2
Reaction #5019
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42026
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42027
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42028
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42029
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 95.8%DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(C)C)C(OC(=O)C(C)C)c1ccc(OC(=O)C(C)C)c2[nH]c(=O)ccc12.Cl.O
Reaction #56067
5-(1-isobutyryloxy-2-isopropylaminobutyl)-8-isobutyryloxycarbostyril hydrochloride monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1
Reaction #75030
alpha-cyano-3-phenoxybenzyl 2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)OC(C#N)c1ccccc1
Reaction #75031
ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC(=O)[C@@]1(c2ccccc2)C[C@H]1CO)[C@@]1(c2ccccc2)C[C@H]1CO
Reaction #82319
compound 1
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC(=O)[C@]1(c2ccccc2)C[C@@H]1CO)[C@]1(c2ccccc2)C[C@@H]1CO
Reaction #82320
compound 13
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC(=O)[C@@]1(c2ccccc2)C[C@H]1CO)[C@@]1(c2ccccc2)C[C@H]1CO
Reaction #82322
compound 25
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C=O)CC.OC[C@@H]1C[C@@H]1c1ccccc1
Reaction #82323
compound 26
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2CCC1CC2
Reaction #200898
DOI: 10.1039/C8SC04228D
CCCCCCCCC1CCC(CCCCCCCC)C(=O)OC1=O
Reaction #207140
DOI: 10.1039/C8SC04228D
CC12CCC(C(=O)N(CCc3ccccn3)C1=O)C2(C)C
Reaction #235939
DOI: 10.1039/C8SC04228D
CCC(=COC(=O)C(CC)CC)CC
Reaction #244254
DOI: 10.1039/C8SC04228D
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