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COC1CNC1

c1ccc(C(OC2CN(CCCOCCc3ccc4sccc4c3)C2)(c2ccccc2)c2ccccc2)cc1
Reaction #7553
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-(trityloxy)azetidine
Ausbeute 36.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1(C(c2cc(F)cc(F)c2)S(C)(=O)=O)CN(C(c2ccccc2)c2ccccc2)C1
Reaction #46347
3-acetoxy-1-benzhydryl-3-[(3,5-difluorophenyl)(methyl-sulfonyl)methyl]azetidine
DOI: 10.6084/m9.figshare.5104873.v1
COC1CN(C(=O)c2cccc3c2nc(C(=O)NC2CCN(C(C)C)CC2)n3CCc2ccc(Cl)cc2)C1
Reaction #46845
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(NC(=O)[C@H](O)c2ccccc2)C(=O)N2C(C(=O)O)=C(C(CCC(=O)O)Sc3nnn[nH]3)CS[C@@H]21
Reaction #55420
7β-D-Mandelamido-7α-methoxy-3-[1-(2-carboxyethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(N)C(=O)N2C(C(=O)OC(C)(C)C)=C(C(CCC(N)=O)Sc3nnn[nH]3)CS[C@@H]21
Reaction #55422
7β-amino-7α-methoxy-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid t-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(OC2CN(c3ccc([C@H](C)NC(C)=O)cc3)C2)c(F)c1
Reaction #68795
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](C)c1ccc(N2CC(Oc3ccc(C(F)(F)F)cn3)C2)cc1
Reaction #68801
(S)—N-(1-{4-[3-(5-Trifluoromethyl-pyridin-2-yloxy)-azetidin-1-yl]-phenyl}-ethyl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](C)c1ccc(N2CC(Oc3ccnc(N4CCOCC4)n3)C2)cc1
Reaction #68806
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC1CN(C(=O)CCNC(=O)C(O)c2ccc(-c3noc(-c4onc(-c5ccccc5)c4C(F)(F)F)n3)cc2)C1
Reaction #164399
(R/S)-2-hydroxy-N-(3-(3-methoxyazetidin-1-yl)-3-oxopropyl)-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.c1ccc(COC2CNC2)cc1
Reaction #170125
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCc2cc(/C=C/C(=O)N3CC(OCc4ccccc4)C3)cnc2N1
Reaction #170126
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.c1csc(COC2CNC2)n1
Reaction #170135
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCc2cc(/C=C/C(=O)N3CC(OCc4nccs4)C3)cnc2N1
Reaction #170136
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(COC2CN(C(c3ccccc3)c3ccccc3)C2)cc1Cl
Reaction #173600
DOI: 10.1039/C8SC04228D
COC(=O)C(=C(C)C)N1C(=O)C(OC(=O)COc2ccccc2)C1SSc1nc2ccccc2s1
Reaction #173700
DOI: 10.1039/C8SC04228D
COc1cc(OC2CN(C(=O)c3nnc(-c4ccccc4)o3)C2)ccc1CN1CCOCC1
Reaction #176545
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCCC(C)(O)CC5)cc4)C3)o2)cc1
Reaction #176603
DOI: 10.1039/C8SC04228D
O=C(c1nc2ccccc2[nH]1)N1CC(Oc2nccnc2C2=CCC(O)CC2)C1
Reaction #185607
DOI: 10.1039/C8SC04228D
CC(C)NC(=O)N1CC(OC(c2ccccc2Cl)c2ccccc2Cl)C1
Reaction #189009
DOI: 10.1039/C8SC04228D
O=C(c1nnc(-c2ccccc2)o1)N1CC(Oc2ccc(CN3CC(C(F)F)C3)cc2)C1
Reaction #194511
DOI: 10.1039/C8SC04228D
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