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735434

O=C(OCC12CCCN(CCC1)C2)c1c[nH]c2ccccc12
Reaction #5482
colorless crystals
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC3C(OC(=O)c4ccccc4)CCC3C2=O)ccc(C#N)c1Cl
Reaction #43466
title compounds 1K
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)CC(=O)N[C@@H](C)C(=O)OCC(C)C
Reaction #51344
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1CC(O)C(O)C1)c1ccc([N+](=O)[O-])cc1
Reaction #69434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #81347
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methyl-butyric acid [11β,21-dihydroxy-3,20-dioxo-9-fluoro-16β-methyl-17-valeroyloxy-pregna -1,4-dien-21-yl] ester
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)c1ccccc1
Reaction #93000
above-identified compound
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)O[C@H]1CN2CCC1CC2
Reaction #164153
(S)-((R)-quinuclidin-3-yl) 2-(tert-butoxycarbonylamino)-3-phenylpropanoate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1CN2CCC1CC2)C(Nc1cccc(OC(F)(F)F)c1)c1ccccc1
Reaction #164166
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(NC(C(=O)O[C@H]2CN3CCC2CC3)c2ccccc2)c1
Reaction #164168
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(c1ccccc1)C(C(=O)O[C@H]1CN2CCC1CC2)c1ccccc1
Reaction #164187
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1CN2CCC1CC2)C(Nc1cccc(F)c1)c1ccc(F)cc1
Reaction #164193
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(Nc2ccccc2)C(=O)O[C@H]2CN3CCC2CC3)cc1
Reaction #164201
desired compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCC(C)C1CCC2(C#N)C3C=CC4C(C)(C)C(OC(=O)c5ccccc5)CCC4(C)C3CCC12C
Reaction #183662
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #196274
DOI: 10.1039/C8SC04228D
CC(=CC(=O)OCC(C)C)n1cncn1
Reaction #200560
DOI: 10.1039/C8SC04228D
CCOC(C)OC1(C)CCC(O[Si](CC)(CC)CC)CC(=O)OC(C(C)=CC=CC(C)CC2OC2C(C)C(CC)OC(=O)c2ccccc2)C(C)C=CC1O
Reaction #204819
DOI: 10.1039/C8SC04228D
CC(=O)OC1C(N2CCCCC2)CC2C3CCC4CCC(=O)CC4(C)C3CCC21C
Reaction #206028
DOI: 10.1039/C8SC04228D
C#CCCCC(=O)OCC1(CCC)COC1
Reaction #216444
(3-propyloxetan-3-yl)methyl hex-5-ynoate
DOI: 10.6084/m9.figshare.5104873.v1
C#CCCCC12OCC(CCC)(CO1)CO2
Reaction #216445
1-(Pent-4-ynyl)-4-propyl-2,6,7-trioxabicyclo[2.2.2]octane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(COC(=O)c1ccccc1)C(COC(=O)c1ccccc1)C(C)C
Reaction #219922
product
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
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