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CN(C)C1CCCCC1N

CC(C)(C)OC(=O)N1C(NCc2ccccc2)=N[C@@H]2CCCC[C@@H]21
Reaction #47024
product 189
Ausbeute 84.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2cccc(F)c2)=N[C@@H]2CCCC[C@@H]21
Reaction #47025
product 191
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2ccc(F)cc2)=N[C@@H]2CCCC[C@@H]21
Reaction #47026
product 193
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2ccc(F)c(F)c2)=N[C@@H]2CCCC[C@@H]21
Reaction #47027
product 195
Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1CCCC[C@H]1C(=O)O
Reaction #54524
cis-2-(dimethylamino)cyclohexanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCNC1CCCCC1N(C)C
Reaction #54525
N,N-Dimethyl-N'-ethyl-1,2-cyclohexanediamine
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCCCC1NCc1ccccc1
Reaction #54527
N,N-dimethyl-N'-benzyl-1,2-cyclohexanediamine
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1N
Reaction #54528
trans-N,N-Dimethyl-1,2-cyclohexanediamine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC(=O)c1ccc(C#N)cc1
Reaction #54532
amide
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC(=O)c1cccc(C(F)(F)F)c1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #54534
amide
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1CCCC[C@H]1N(C)C
Reaction #54535
trans-N,N,N'-Trimethyl-1,2-cyclohexanediamine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC=O
Reaction #54536
trans-N-[2-(Dimethylamino)-cyclohexyl]-formamide
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H]1CCCC[C@H]1N(C)C
Reaction #54538
amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCN([C@H]2CCCC[C@H]2NC(=O)c2cc(C)cc(C)c2)C1
Reaction #54539
cis-N-[2-(3-acetyloxy-1-pyrrolidinyl)cyclohexyl]-3,5-dimethylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1C[C@@H]2C[C@@H]2[C@H]1N1C(=O)c2ccccc2C1=O
Reaction #84686
crude compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)N[C@H]1C[C@@H]2C[C@@H]2[C@H]1N1C(=O)c2ccccc2C1=O
Reaction #84687
title compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(O)cc(-n2nc(C(C)(C)C)cc2N)c1
Reaction #88922
title compound
Ausbeute 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H](COc2ccc3c(c2)C(C)(C)c2[nH]c4cc(I)ccc4c2C3=O)[C@@H](CO[Si](C)(C)C(C)(C)C)O1
Reaction #90124
title compound
Ausbeute 70.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(F)c1-n1ccnn1
Reaction #92491
3-fluoro-2-(1H-1,2,3-triazol-1-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1CCCC[C@@H]1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162114
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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