An 29 Reaktionen beteiligt

1130757

CS(=O)(=O)Nc1cc(C(O)CNCCc2ccc(NC3CCN(c4ccc(S(=O)(=O)N5CCCCC5)cc4)CC3)cc2)ccc1O
Reaction #251285
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C[Si](C)(C)C[Si](C)(Cl)Cl
Reaction #414557
(trimethylsilylmethyl)methyldichlorosilane
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
COC(=O)[C@@H]1CCCN1C(=O)N1CCC(Nc2ccc(CCNC[C@H](O)c3ccc(O)cc3NS(C)(=O)=O)cc2)CC1
Reaction #483236
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCOC(=O)C1CCCN(C(=O)N2CCC(Nc3ccc(CCNC[C@H](O)c4ccc(O)c(NS(C)(=O)=O)c4)cc3)CC2)C1
Reaction #483237
title compound
Ausbeute 4.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CS(=O)(=O)Nc1cc([C@@H](O)CNCCc2ccc(NC3CCN(C(=O)c4ccc(C(=O)O)cc4)CC3)cc2)ccc1O
Reaction #483264
title compound
Ausbeute 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCCCCCCCNC(=O)Nc1ccc(S(=O)(=O)N2CCC(Nc3ccc(CCNC[C@H](O)c4ccc(O)c(NS(C)(=O)=O)c4)cc3)CC2)cc1
Reaction #483273
title compound
Ausbeute 13.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CS(=O)(=O)Nc1cc([C@@H](O)CNCCc2ccc(NC3CCN(c4ccc(S(=O)(=O)N5CCCCC5)cc4)CC3)cc2)ccc1O
Reaction #483277
title compound
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCOC(=O)c1ccc(N2CCC(Nc3ccc(CCNC[C@H](O)c4ccc(O)c(NS(C)(=O)=O)c4)cc3)CC2)cc1
Reaction #483278
4-[4-(4-{2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-methanesulfonylamino-phenyl)-ethylamino]-ethyl}-phenylamino)-piperidin-1-yl]-benzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CC(C)(CC[SiH](Cl)Cl)c1ccccc1
Reaction #574948
neophylmethyldichlorosilane
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
CCC(C)C[Si](C)(Cl)Cl
Reaction #761707
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC[C@H](C)C[Si](C)(Cl)Cl
Reaction #814009
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CC1=C(C)C([Si](C)(Cl)Cl)C(C)=C1C
Reaction #928293
tetramethylcyclopentadienyl methyl silicon dichloride
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CS(=O)(=O)Nc1cc(C(O)CNCCc2ccc(NC3CCN(c4nc(-c5ccccc5)cs4)CC3)cc2)ccc1O
Reaction #1025159
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC(=O)Nc1nc(C)c(S(=O)(=O)N2CCC(Nc3ccc(CCNCC(O)c4ccc(O)c(NS(C)(=O)=O)c4)cc3)CC2)s1
Reaction #1040837
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC1=C(C)C([Si](C)(Cl)Cl)C(C)=C1C
Reaction #1091601
tetramethylcyclopentadienyl methyl silicon dichloride
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_04
COc1ccc(C[Si](C)(Cl)Cl)cc1
Reaction #1339922
desired product
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_05
C[Si](Cl)(Cl)Cl
Reaction #1351362
MeSiCl3
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CS(=O)(=O)Nc1cc([C@@H](O)CNCCc2ccc(NC3CCN(C(=O)NCc4cc(F)ccc4F)CC3)cc2)ccc1O
Reaction #1368761
title compound
Ausbeute 46.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
COC(=O)[C@@H]1CCCN1C(=O)N1CCC(Nc2ccc(CCNC[C@H](O)c3ccc(O)cc3NS(C)(=O)=O)cc2)CC1
Reaction #1368762
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
CCOC(=O)C1CCCN(C(=O)N2CCC(Nc3ccc(CCNC[C@H](O)c4ccc(O)c(NS(C)(=O)=O)c4)cc3)CC2)C1
Reaction #1368763
title compound
Ausbeute 4.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
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