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OB(O)c1cccc(Cl)c1

COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #597
Ausbeute 2.3%
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #598
Ausbeute 0.0%
CC1(C)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #7079
title compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #7086
5-(3-chloro-phenyl)-3-methoxy-3-methyl-1,3-dihydro-indol-2-one
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC#CC1(OC)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #7088
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(-c3cccc(Cl)c3)ccc2N1
Reaction #7089
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2ccc(-c3ccc(F)c(Cl)c3)cc21
Reaction #7104
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #9417
subtitled compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #9425
5-(3-chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-one
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c1c(-c1cccc(Cl)c1Cl)cc1[nH]c3ccc(O)cc3c21
Reaction #11117
4-(2,3-dichlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(B(O)O)cc1Cl
Reaction #44349
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2cc(Cl)ccc2O)OC1(C)C
Reaction #44354
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(Cl)cc1B1OC(C)(C)C(C)(C)O1)C(=O)OC(C)(C)C
Reaction #44355
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cc(Cl)ccc2OCc2ccccc2)cc1C(F)(F)F)N1CCCC1
Reaction #44365
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2cc(Cl)ccc2OCc2ccccc2)OC1(C)C
Reaction #44375
2-[5-chloro-2-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(Cl)cc1B(O)O)C(=O)O
Reaction #44376
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C#N)CC(c2cccc(Cl)c2)=C(F)C(O)=C1N
Reaction #45877
compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cccc(Cl)c2)CC1
Reaction #48133
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccc(Cl)c(Cl)c2)CC1
Reaction #48139
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCOCC2)n3-c2ccc(Cl)c(Cl)c2)CC1
Reaction #48146
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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