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39002

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Reaction #5959
oil
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN=C1CCOCC1
Reaction #41159
N′-(tetrahydro-pyran-4-ylidene)-hydrazinecarboxylic acid tert-butyl ester
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNC1CCOCC1
Reaction #41160
(tetrahydro-pyran-4-yl)-hydrazine hydrochloride
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nc3nn(CCCOC4CCCCO4)cc3c(-c3ccco3)c2-c2ccncc2)cc1
Reaction #70902
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CC(O)CC(=O)O)[C@@H](Cc1ccc(Cl)c(Cl)c1)OC(=O)c1ccc2ccccc2c1
Reaction #81129
above-identified compound
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CN(C)C(=O)OC(C)(C)C)CCOCC1
Reaction #86626
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4cn(C5CCOCC5)nn4)cnc32)c1
Reaction #92436
crude product
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4cn(C5CCOCC5)nn4)cnc32)c1
Reaction #92440
N-(2′,4′-difluoro-5-(6-(1-(tetrahydro-2H-pyran-4-yl)-1H-1,2,3-triazol-4-yl)-3H-imidazo[4,5-b]pyridin-3-yl)-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc2ncccc2c1)c1cnc2ccc(-c3cnn(CCO)c3)nn12
Reaction #156400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1cc2cccnc2cc1F)c1cnc2ccc(-c3cnn(CCO)c3)nn12
Reaction #156448
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1cc2cccnc2cc1F)c1cnc2ccc(-c3cnn(CCOC4CCCCO4)c3)nn12
Reaction #156449
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc2ncc(Br)n2c1)c1cnc2ccc(-c3cnn(CCO)c3)nn12
Reaction #156489
(rac)-2-(4-{3-[1-(3-Bromo-imidazo[1,2-a]pyridin-6-yl)-ethyl]-imidazo[1,2-b]pyridazin-6-yl}-pyrazol-1-yl)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@@H]1CC[C@@H](Nc2ccc(F)cc2)[C@]2(O)CCCO[C@H]12
Reaction #160827
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(-c3nc4cc([N+](=O)[O-])ccc4o3)ccc2n1C1CCOCC1
Reaction #161415
title compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(NC(=O)OC(C)(C)C)CCOCC1
Reaction #165918
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(NC(=O)OC(C)(C)C)CCOCC1
Reaction #165924
title compound
Ausbeute 31.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)N(C)C1CN(C(=O)C2CCOCC2)CC1c1ccc(F)cc1)c1cc(Br)cc(C(F)(F)F)c1
Reaction #179102
DOI: 10.1039/C8SC04228D
CC(C)c1nc(N(C)S(C)(=O)=O)nc(-c2ccc(F)cc2)c1C=CC1CC(O[Si](C)(C)C(C)(C)C)CC(=O)O1
Reaction #184151
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1(C(=O)NC(Cc2ccc(I)cc2)C(N)=O)CCOCC1
Reaction #201557
DOI: 10.1039/C8SC04228D
CN(C(=O)N(C)C1CN(C(=O)C2CCOCC2)CC1c1ccc(Cl)c(Cl)c1)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #208231
DOI: 10.1039/C8SC04228D
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