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1319980

CC(=O)NC(=Cc1ccc(C#N)cc1)C(=O)N[C@H](C(=O)O)C1CCCCC1
Reaction #7297
(S)-2-[2-Acetylamino-3-(4-cyanophenyl)acryloylamino]-2-cyclohexylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCCC2CC(CC)OC12O
Reaction #40887
desired title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCCC(=O)C1
Reaction #42601
(3-Oxo-cyclohexyl)-acetic acid
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CNC[C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)CC2CCCC(=O)C2)c1
Reaction #42602
N-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-2-(3-oxocyclohexyl)acetamide
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](CO)CN1CCc2cc(F)ccc21)O[C@@H](CC1CCCCC1)C(=O)N1CCOCC1
Reaction #43551
title compound
Ausbeute 71.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC(c1ccccc1)c1ccccc1)C1=C(COCCC2CCCCC2)NC(c2ccccc2)=NC1c1cccc(Cl)c1
Reaction #52874
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC=Cc1ccccc1)C1=C(COCCC2CCCCC2)NC(c2ccccc2)=NC1c1cccc(Cl)c1
Reaction #52875
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC1(CC(=O)OCc2ccccc2)CCCCC1
Reaction #58790
product ( 6 )
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCCC(O)(c2ccccc2)C1
Reaction #75355
title compound
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCC(CC(=O)O)CC1
Reaction #79874
2-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}acetic acid
Ausbeute 84.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCC(CCO)CC1
Reaction #79875
2-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}-1-ethanol
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)CC1CCC(n2cc(-c3ccc(Oc4ccccc4)cc3)c3c(N)ncnc32)CC1
Reaction #79878
N1-methyl-2-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}acetamide
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1(O)CC=C2C[C@@H]3[C@@H]4C=C[C@H](O)[C@@H]5OC1=C2[C@]45CCN3C
Reaction #82145
3-acetylmorphine
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23C4=C5O[C@H]2[C@@H](O)C=C[C@H]3[C@H]1CC4=CCC5(O)[Si](C)(C)C(C)(C)C
Reaction #82146
product
Ausbeute 56.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-n1ncc2c(=O)[nH]c(CC3CCC(C)CC3)nc21
Reaction #156117
6-[(4-Methylcyclohexyl)methyl]-1-(2-methylphenyl)-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCC(=O)CC1
Reaction #160039
(4-Oxo-cyclohexyl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCC(CC(=O)O)CC1
Reaction #160040
(4-Hydroxy-4-methyl-cyclohexyl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@]1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162196
63a
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCC(c2ccc(-c3ccc(Nc4ccn(C)n4)cn3)cc2)CC1
Reaction #163244
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2ccc(-c3ccc(C4CCC(CC(=O)O)CC4)cc3)nc2)nc1
Reaction #163250
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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