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O=C(O)CCCC1CCCCC1

COC(=O)[C@@H]1C[C@H](NS(=O)(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40606
43
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C[C@@H](CC1CCC2(CC1)CC2)C(=O)N1C(=O)OC[C@@H]1Cc1ccccc1
Reaction #43568
4-(4-(S)-Benzyl-2-oxo-oxazolidin-3-yl)-4-oxo-3-(R)-spiro[2.5]oct-6-ylmethyl-butyric acid
Ausbeute 278.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C12CC3CC(CC(C3)C1)C2
Reaction #46044
α-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=O)C12CC3CC(CC(O)(C3)C1)C2
Reaction #46045
Formula 1a
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC[C@H]1CC[C@H](N(C)C(=O)OC(C)(C)C)CC1
Reaction #53899
trans-4-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexyl]-butyric acid ethyl ester
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](CCCCO)CC1
Reaction #53900
trans-[4-(4-Hydroxy-butyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C12CC3CC(CC(C3)C1)C2
Reaction #57411
a-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66028
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66029
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66030
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(C2CCCCC2(CC(=O)OC)C(=O)C2(CC(=O)OC)CCCCC2c2ccc(NC)c(NC(=O)COc3ccc(C#N)cc3)c2)cc1NC(=O)COc1ccc(C#N)cc1
Reaction #78606
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC1CCC(c2ccc(-c3cnc(Nc4cccc(Cl)c4)o3)cc2)CC1
Reaction #163220
title compound
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172730
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172731
title compound
Ausbeute 68.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)O[Si](C)(C)C(C)(C)C)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172732
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172733
title compound
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N=C=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172734
title compound
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)c(F)c6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172872
title compound
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)c(F)c6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172873
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H]2CC[C@]3(C)[C@H]4CC[C@@H]5[C@H]6[C@H](C(C)C)CC[C@]6(C(=O)O)CC[C@@]5(C)[C@]4(C)CC[C@H]3C2(C)C)cc1
Reaction #172885
title compound
Ausbeute 82.2%DOI: 10.6084/m9.figshare.5104873.v1
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