Recherche de Sous-structure

434467

$CC(C)(C)OC(=O)NCc1cnn(C[C@H]2NC(=O)[C@H]2NC(=O)/C(=N\OC2(C(=O)OC(c3ccccc3)c3ccccc3)CC2)c2csc(NC(=O)OC(C)(C)C)n2)n1$

Reaction #795566

title compound

Rendement 84.3%DOI: 10.6084/m9.figshare.5104873.v1

$NCc1cnn(C[C@@H]2[C@H](NC(=O)/C(=N\OC3(C(=O)O)CC3)c3csc(N)n3)C(=O)N2S(=O)(=O)O)n1$

Reaction #795567

title compound

Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1

$CC(C)(O/N=C(\C(=O)N[C@@H]1C(=O)N(S(=O)(=O)O)[C@@H]1Cn1ncc(CN)n1)c1csc(N)n1)C(=O)O$

Reaction #795604

title compound

Rendement 31.1%DOI: 10.6084/m9.figshare.5104873.v1

Nc1nc(/C(=N/OC2(C(=O)O)CC2)C(=O)N[C@@H]2C(=O)N(S(=O)(=O)O)[C@@H]2Cn2ncc(CNCC3CNC3)n2)cs1

Reaction #795641

1-(((Z)-(1-(2-aminothiazol-4-yl)-2-(((2R,3S)-2-((4-(((azetidin-3-ylmethyl)amino)methyl)-2H-1,2,3-triazol-2-yl)methyl)-4-oxo-1-sulfoazetidin-3-yl)amino)-2-oxoethylidene)amino)oxy)cyclopropanecarboxylic acid

DOI: 10.6084/m9.figshare.5104873.v1

$NCCCNCc1cnn(C[C@@H]2[C@H](NC(=O)/C(=N\OC3(C(=O)O)CC3)c3csc(N)n3)C(=O)N2S(=O)(=O)O)n1$

Reaction #795651

title compound

Rendement 43.7%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)Nc1nc(/C(=N/OC2(C(=O)OC(c3ccccc3)c3ccccc3)CC2)C(=O)N[C@@H]2C(=O)N(S(=O)(=O)O)[C@@H]2Cn2nc(CN)c(CN(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)n2)cs1

Reaction #795668

title compound

DOI: 10.6084/m9.figshare.5104873.v1

$NCc1nn(C[C@@H]2[C@H](NC(=O)/C(=N\OC3(C(=O)O)CC3)c3csc(N)n3)C(=O)N2S(=O)(=O)O)nc1CN$

Reaction #795669

title compound

Rendement 19.0%DOI: 10.6084/m9.figshare.5104873.v1

$CC(C)(C)OC(=O)N=C(N1CC(CNC(=O)OC(C)(C)C)C1)N(Cc1cnn(C[C@H]2NC(=O)[C@H]2NC(=O)/C(=N\OC2(C(=O)OC(c3ccccc3)c3ccccc3)CC2)c2csc(NC(=O)OC(C)(C)C)n2)n1)C(=O)OC(C)(C)C$

Reaction #795684

title compound

Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1

$N=C(NCc1cnn(C[C@@H]2[C@H](NC(=O)/C(=N\OC3(C(=O)O)CC3)c3csc(N)n3)C(=O)N2S(=O)(=O)O)n1)N1CC(CN)C1$

Reaction #795685

title compound

Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1

$C[n+]1cccc(CN(Cc2cnn(C[C@H]3NC(=O)[C@H]3NC(=O)/C(=N\OC3(C(=O)OC(c4ccccc4)c4ccccc4)CC3)c3csc(NC(=O)OC(C)(C)C)n3)n2)C(=O)OC(C)(C)C)c1.[Cl-]$

Reaction #795692

3-((((2-(((2R,3S)-3-((Z)-2-((1-((benzhydryloxy)carbonyl)cyclopropoxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidin-2-yl)methyl)-2H-1,2,3-triazol-4-yl)methyl)(tert-butoxycarbonyl)amino)methyl)-1-methylpyridin-1-ium chloride

DOI: 10.6084/m9.figshare.5104873.v1

$C[n+]1cccc(CNCc2cnn(C[C@@H]3[C@H](NC(=O)/C(=N\OC4(C(=O)O)CC4)c4csc(N)n4)C(=O)N3S(=O)(=O)[O-])n2)c1$

Reaction #795693

title compound

Rendement 38.6%DOI: 10.6084/m9.figshare.5104873.v1

$Cc1nn(C[C@H]2NC(=O)[C@H]2NC(=O)/C(=N\OC2(C(=O)OC(c3ccccc3)c3ccccc3)CC2)c2csc(NC(=O)OC(C)(C)C)n2)nc1CNC(=O)OC(C)(C)C$

Reaction #795698

title compound

Rendement 82.6%DOI: 10.6084/m9.figshare.5104873.v1

$Cc1nn(C[C@@H]2[C@H](NC(=O)/C(=N\OC3(C(=O)O)CC3)c3csc(N)n3)C(=O)N2S(=O)(=O)O)nc1CN$

Reaction #795699

title compound

Rendement 59.5%DOI: 10.6084/m9.figshare.5104873.v1

CC(c1cnn(C[C@H]2NC(=O)[C@H]2NC(=O)OCc2ccccc2)n1)N(C(=O)OC(C)(C)C)/C(=N/C(=O)OC(C)(C)C)n1cccn1

Reaction #795707

title compound

Rendement 22.4%DOI: 10.6084/m9.figshare.5104873.v1

$CC(NC(=N)NCCCN)c1cnn(C[C@@H]2[C@H](NC(=O)/C(=N\OC3(C(=O)O)CC3)c3csc(N)n3)C(=O)N2S(=O)(=O)O)n1$

Reaction #795708

title compound

Rendement 39.8%DOI: 10.6084/m9.figshare.5104873.v1

$C[C@@H](c1cnn(C[C@H]2NC(=O)[C@H]2NC(=O)/C(=N\OC2(C(=O)OC(c3ccccc3)c3ccccc3)CC2)c2csc(NC(=O)OC(C)(C)C)n2)n1)N(CCCNC(=O)OC(C)(C)C)C(=O)OC(C)(C)C$

Reaction #795711

desired compound

Rendement 96.3%DOI: 10.6084/m9.figshare.5104873.v1

$C[C@H](NCCCN)c1cnn(C[C@@H]2[C@H](NC(=O)/C(=N\OC3(C(=O)O)CC3)c3csc(N)n3)C(=O)N2S(=O)(=O)O)n1$

Reaction #795712

title compound

Rendement 25.8%DOI: 10.6084/m9.figshare.5104873.v1

COc1ccc(CN2C(=O)[C@@H](NC(=O)OCc3ccccc3)[C@H]2Cn2nc3c(n2)CN(C(=O)OC(C)(C)C)C3)c(OC)c1

Reaction #795722

title compound

Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1Cc2nn(C[C@H]3NC(=O)[C@H]3NC(=O)OCc3ccccc3)nc2C1

Reaction #795723

product

Rendement 51.8%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1Cc2nn(C[C@H]3NC(=O)[C@H]3N)nc2C1

Reaction #795724

tert-Butyl 2-(((2R,3S)-3-amino-4-oxoazetidin-2-yl)methyl)-4,6-dihydropyrrolo[3,4-d][1,2,3]triazole-5(2H)-carboxylate

DOI: 10.6084/m9.figshare.5104873.v1

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