Substructure Search

11264

N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2848
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1CN(CCCOCCc2csc3ccccc23)C1
Reaction #7537
1-{3-[2-(1-benzothiophen-3-yl)ethoxy]propyl}-3-azetidinol
Yield 48.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2ccccc2C(=O)O)nn1CCC(C)(C)NCC(O)c1cc(O)cc2c1OCC(=O)N2
Reaction #58092
1-{3-[2-hydroxy-2-(6-hydroxy-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-ethylamino]-3-methyl-butyl}-5-methyl-1H-[1,2,4]triazol-3-yl-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C1=C(C(=O)[O-])N2C(=O)C(NC(=O)C(=NOC(F)F)c3csc(N)n3)[C@H]2SC1)[NH+]1CCCC1
Reaction #62778
7-[2-(2-aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(1-methyl-1-pyrrolidiniomethyl)-3-cephem-4-carboxylate
Yield 72.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CCN=C2
Reaction #66588
title product
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CNC(=O)c1ccc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74478
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
OCCCC#Cc1cc2c(cc1F)NCC2
Reaction #77793
5-(6-Fluoro-2,3-dihydro-1H-indol-5-yl)-pent-4-yn-1-ol
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cc(N2CCN(CCNC(=O)OC(C)(C)C)CC2)ccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1
Reaction #86487
title compound
Yield 54.4%DOI: 10.6084/m9.figshare.5104873.v1
O=S1CCc2nc(N3CCN(c4ccc(Cl)cc4)CC3)nc(N3C[C@H](O)C[C@H]3CO)c21
Reaction #157279
product
Yield 75.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)Nc2ccc(N3CCN(c4nc5c(c(Nc6cccc(Cl)c6)n4)S(=O)CC5)CC3)cc2)cn1.O=C(O)C(F)(F)F
Reaction #157296
product
Yield 57.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2ncsc2c1)N1CCNCC1COc1cccnc1
Reaction #157337
title compound
Yield 85.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(Nc1ccc2c(c1)CCC2)N1CCNCC1COc1cccnc1
Reaction #157341
title compound
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(c1ccc(-c2ccccc2Cl)o1)N1CCNCC1COc1cccnc1
Reaction #157353
desired product
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cncc(OCC2CNCCN2c2nc3ccccc3o2)c1
Reaction #157386
2-(2-((pyridin-3-yloxy)methyl)piperazin-1-yl)benzo[d]oxazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(N3CCNCC3COc3cccnc3)oc2c1.Cl
Reaction #157387
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(N3CCNCC3COc3cccnc3)oc2c1.Cl
Reaction #157388
desired product
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1CCNC[C@H]1C.O=C(O)C(F)(F)F
Reaction #167935
racemic (cis)-4-methoxy-3-methylpiperidine 2,2,2-trifluoroacetate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COC(=O)C2=C(CSc3nc4cn(C)ccc-4[n+]3C)CS[C@@H]3C(NC(=O)/C(=N\O[C@@H](C)C(=O)OC(c4ccccc4)c4ccccc4)c4csc(NC(c5ccccc5)(c5ccccc5)c5ccccc5)n4)C(=O)N23)cc1.O=C([O-])C(F)(F)F
Reaction #216064
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O/N=C(\C(=O)NC1C(=O)N2C(C(=O)[O-])=C(CSc3nc4cn(C)ccc-4[n+]3C)CS[C@H]12)c1csc(N)n1)C(=O)O
Reaction #216065
title compound
Yield 52.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OOC(=O)C(F)(F)F)C(F)(F)F
Reaction #272548
DOI: 10.1039/C8SC04228D
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