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C[C@@H](C=O)[C@H]1COC(=O)N1Cc1ccccc1

Reaction #85656

(R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)propanal

Rendimiento 105.3%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)NS(=O)(=O)c1ccc(CN(CCc2ccc(Br)cc2)C2CCN(C(=O)OC(C)(C)C)CC2)cc1

Reaction #88069

tert-butyl 4-((4-(N-acetylsulfamoyl)benzyl)(4-bromophenethyl)amino)piperidine-1-carboxylate

Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1

CCCOC(=O)[C@H](Cc1ccc(-c2c(C)n(C)c(=O)n(C)c2=O)cc1)NC(=O)c1c(F)cc(CNCc2cc(F)c(C(=O)N[C@@H](Cc3ccc(-c4c(C)n(C)c(=O)n(C)c4=O)cc3)C(=O)OCCC)c(F)c2)cc1F

Reaction #92029

Rendimiento 39.2%DOI: 10.6084/m9.figshare.5104873.v1

Cc1c(-c2ccc(C[C@H](NC(=O)c3c(F)cc(CNCc4cc(F)c(C(=O)N[C@@H](Cc5ccc(-c6c(C)n(C)c(=O)n(C)c6=O)cc5)C(=O)O)c(F)c4)cc3F)C(=O)O)cc2)c(=O)n(C)c(=O)n1C

Reaction #92030

Rendimiento 75.1%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)[C@H](Cc1ccc(-c2c(C)n(C)c(=O)n(C)c2=O)cc1)NC(=O)c1c(F)cc(CNCc2cc(F)c(C(=O)N[C@@H](Cc3ccc(-c4c(C)n(C)c(=O)n(C)c4=O)cc3)C(=O)OC)c(F)c2)cc1F

Reaction #92031

DOI: 10.6084/m9.figshare.5104873.v1

Br.CCC(C)n1c(-c2ccc(Cl)c(S(=O)(=O)N(C)C)c2)csc1=Nc1ccccc1

Reaction #96043

3-sec.-Butyl-4-(4-chloro-3-dimethylsulfamoylphenyl)-2-phenylimino-4-thiazoline hydrobromide

DOI: 10.6084/m9.figshare.5104873.v1

$COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(N)c(OC)n2)c(OC)c1$

Reaction #157828

(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one

DOI: 10.6084/m9.figshare.5104873.v1

COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)ccc1N

Reaction #157829

(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]pyrrolidin-2-one

Rendimiento 44.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #158169

Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1

Cc1ccc(CNC(C(=O)O[C@H]2C[N+]3(CC(=O)c4cccs4)CCC2CC3)c2ccccc2)cc1.Cc1ccc(CNC(C(=O)O[C@H]2C[N+]3(CC(=O)c4cccs4)CCC2CC3)c2ccccc2)cc1.O=C[O-].O=C[O-]

Reaction #164225

Rendimiento 78.6%DOI: 10.6084/m9.figshare.5104873.v1

COc1ccc(CNC(C(=O)O[C@H]2C[N+]3(CC(=O)c4cccs4)CCC2CC3)c2ccccc2)cc1.COc1ccc(CNC(C(=O)O[C@H]2C[N+]3(CC(=O)c4cccs4)CCC2CC3)c2ccccc2)cc1.O=C[O-].O=C[O-]

Reaction #164226

Rendimiento 76.1%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)NC(=O)c1ccc2c(c1)OCCc1cc(C(=O)N(C)c3ccc(C(=O)N(C)C)cc3Cl)sc1-2

Reaction #171812

DOI: 10.6084/m9.figshare.5104873.v1

O=C(NC1CCC(CCN2CCN(c3nccc4c3CCO4)CC2)CC1)c1ccc(Cl)cc1

Reaction #178891

DOI: 10.1039/C8SC04228D

CC(C)(C)OC(=O)N1CCC(CCNc2ncc(Br)c(-c3cc4c(C(=O)NC5CC5)cccc4s3)n2)CC1

Reaction #192375

DOI: 10.1039/C8SC04228D

CN(Cc1ccc(NC(=O)C2=Cc3cc(-c4ccc5c(c4)CCCO5)ccc3S(=O)(=O)CC2)cc1)C1CCOCC1

Reaction #198656

DOI: 10.1039/C8SC04228D

COc1cccc(CNCC(O)C(Cc2cc(F)cc(F)c2)NC(=O)c2cc(C(C)=O)cc(S(C)(=O)=O)c2)c1

Reaction #200966

DOI: 10.1039/C8SC04228D

CC(C)C1CCc2ncnc(N3CC4(CCNCC4)c4c(CN(C(=O)OC(C)(C)C)C5CCCC5)cccc43)c21

Reaction #202918

DOI: 10.1039/C8SC04228D

COc1c2ccc(NC(C)=O)cc2nn1CC(C)(C#N)NC(=O)c1ccc(OC(F)(F)F)cc1

Reaction #205848

DOI: 10.1039/C8SC04228D

CSc1ccc(Br)c(CN2C(=O)OC(c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2C)c1

Reaction #209292

DOI: 10.1039/C8SC04228D

CC(=O)O[C@H]1C(=O)[C@@]2(C)[C@H]([C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)c4ccccc4)c4ccccc4)C(C)=C1C3(C)C)[C@]1(OC(C)=O)CO[C@@H]1C[C@@H]2O

Reaction #218931

DOI: 10.6084/m9.figshare.5104873.v1

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