Busqueda de Subestructura

4187

C#CC12CCCN1CCC2
Reaction #3396
oil
Rendimiento 71.3%DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])(O)O.O=P([O-])([O-])O.[Cl-].[Cl-].[K+].[K+].[Na+].[Na+].[Na+]
Reaction #4257
phosphate buffered saline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC/C(C)=C/CC/C(C)=C/CC/C=C(\C)CC/C=C(\C)CCC=C(C)C
Reaction #52137
MF59
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1cc(CCC#N)ccc1-c1ccc(-c2ccc(OCC#N)c(Cc3ccccc3)c2)c(Cc2ccccc2)c1
Reaction #54110
29
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1cc(CCC(=O)O)ccc1-c1ccc(-c2ccc(OCC(=O)O)c(Cc3cccc4ccccc34)c2CC(C)C)cc1
Reaction #54126
3-(4-(Carboxymethoxy)-2,2″-diisobutyl-3-naphthalen-1-ylmethyl-[1,1′:4′,1″]-terphenyl-4″-yl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)C(O)(CC)c1cc[nH]c(=O)c1CO
Reaction #58769
title compound
Rendimiento 61.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21
Reaction #64837
Biotin
DOI: 10.6084/m9.figshare.5104873.v1
N#CCn1cc(-c2ccnc3c2cnn3C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
Reaction #72958
2-(4-(1-trityl-1H-pyrazolo[3,4-b]pyridin-4-yl)-1H-pyrazol-1-yl)ethanenitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@H]1CCN(C(=O)OCc2ccccc2)C1
Reaction #78413
desired product
Rendimiento 70.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(-c2ccccc2OC)c1
Reaction #82475
methyl 3-(2-methoxyphenyl)benzoate
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(F)F)[C@H]1COC(=O)N1c1ccnc(F)n1
Reaction #85658
(S)-4-((R)-1,1-difluoropropan-2-yl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-one
Rendimiento 58.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(F)F)[C@H]1COC(=O)N1c1nc(Cl)ncc1F
Reaction #85659
(S)-3-(2-chloro-5-fluoropyrimidin-4-yl)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one
Rendimiento 65.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(OCCOC2CCCCO2)cc1[N+](=O)[O-]
Reaction #86489
title compound
Rendimiento 38.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)O)S(=O)(=O)CC1CCOCC1
Reaction #160419
2-methyl-2-(tetrahydro-pyran-4-ylmethanesulfonyl)-propionic acid
Rendimiento 105.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(-c4ccc(C(O)CO)cc4)o3)n2)cc1
Reaction #165825
product
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)CCN1CCN(CCO)CC1.[Cl-].[Na+]
Reaction #167530
HEPES NaCl
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])(O)O.O=P([O-])([O-])O.[Cl-].[Cl-].[K+].[K+].[Na+].[Na+].[Na+]
Reaction #314696
Phosphate Buffered Saline
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])(O)O.O=P([O-])([O-])O.[Cl-].[Cl-].[K+].[K+].[Na+].[Na+].[Na+]
Reaction #319690
Phosphate buffered saline
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #326414
Sn-Beta zeolite
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(/C=C2\c3ccccc3COc3cc(F)ccc32)ccc1N[C@@H]1C[C@@H]2COCCN2C1
Reaction #331535
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
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