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CC(N)CO

CC(N)COc1ccc(C#N)cc1
Reaction #1022
desired product
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)COc1ccncc1
Reaction #1023
desired product
Ausbeute 30.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](CO)C(C)C
Reaction #5035
N-Methyloxycarbonyl-D-valinol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)NCc1cccc(-c2ccnc(Cl)n2)c1
Reaction #43125
2-(S)-[3-(2-Chloro-pyrimidin-4-yl)-benzylamino]-propan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](CO)NC(=O)[C@@H](CC(=O)N1CCOCC1)c1ccc(F)cc1
Reaction #43563
2-(S)-(4-Fluoro-phenyl)-N-(1-(S)-hydroxymethyl-2-methyl-propyl)-4-morpholin-4-yl-4-oxo-butyramide
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)NCc1ccc2c(c1)cc(-c1ccc(Cl)c3c1C(=O)NC3)n2C(=O)OC(C)(C)C
Reaction #49314
4-chloro-7-{1-(tert-butoxycarbonyl)-5-[(2-hydroxy-1-methylethyl)aminomethyl]indol-2-yl}isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)NC(=N)c1c(O)nsc1Nc1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #62042
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)NC(=N)c1c(O)nsc1Nc1ccc(C(=O)C2CNc3ccccc32)cc1
Reaction #62045
5-[4-(2,3-dihydro-indole-1-carbonyl)-phenylamino]-3-hydroxy-N-(2-hydroxy-1-methyl-ethyl)-isothiazole-4-carboxamidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](CO)NC(=O)c1cc(F)c2[nH]nc(/C=C/c3cccnc3)c2c1
Reaction #62306
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)NC(C)CO
Reaction #62582
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CO)Nc1nc(Cl)ncc1I
Reaction #66491
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3nc(N[C@@H](CO)C(C)C)ncc3C#N)c3cc(C)cnc32)cc1
Reaction #69150
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CO)NC(=O)c1ccc(OCc2ccc(C3CCN(C(=O)OC(C)(C)C)CC3)cn2)cc1F
Reaction #70427
title compound
Ausbeute 87.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)NC(C)CO
Reaction #72236
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(CO)NC(=O)c1nsc2ccc(-n3c(=O)cc(C(F)(F)F)n(C)c3=O)cc12
Reaction #77263
title compound
Ausbeute 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)N1CCN(c2cccc3c2OCCO3)CC1
Reaction #79483
IV
DOI: 10.6084/m9.figshare.5104873.v1
N
Reaction #79581
ammonia
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](CO)NC(=O)OCc1ccccc1
Reaction #81391
N-benzyloxycarbonyl-valinol
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](CO)Nc1nc(N2CCN(c3ccc(Cl)cc3)CC2)nc2c1S(=O)CC2
Reaction #157283
(R)-2-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-4-ylamino}-3-methyl-butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](CO)NC(=O)C1(NC(=O)c2ccco2)CCCCC1
Reaction #161027
title compound
Ausbeute 74.7%DOI: 10.6084/m9.figshare.5104873.v1
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