Teilstruktursuche

1397832

CCO[C@@H](Cc1ccc(OCCc2ccc(OS(C)(=O)=O)cc2)cc1)C(=O)O
Reaction #7074
(S)-2-Ethoxy-3-[4-[[4-(methylsulphonyloxy)phenethyl]oxy]phenyl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(Oc2ccc(CC3SC(=O)NC3=O)cc2)cc1)NC(=O)C1CCCN1C(=O)OC(C)(C)C
Reaction #7446
crude compound
Ausbeute 51.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(Oc2ccc(CC3SC(=O)NC3=O)cc2)cc1)NC(=O)C(C)NC(=O)OC(C)(C)C
Reaction #7447
title compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](Cc1cc(I)c(Oc2cc(I)c(O)c(I)c2)c(I)c1)NC(=O)C(F)(F)F
Reaction #56344
thyroxine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(C(=O)O)S(C)(=O)=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77814
aimed product
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #87144
(2S,3R)-benzyl 2-((tert-butoxycarbonyl)amino)-3-hydroxy-3-(4-methoxyphenyl)propanoate
Ausbeute 71.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](N)C(=O)OCc2ccccc2)cc1
Reaction #87145
(2S,3R)-benzyl 2-amino-3-hydroxy-3-(4-methoxyphenyl)propanoate
Ausbeute 101.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1c(F)cc(CCC(=O)O)cc1F
Reaction #91198
title compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Cc1ccc(OCc2cc(C)cnc2SC(C)C)cc1
Reaction #91199
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1ncccc1COc1c(F)cc(CCC(=O)OCC)cc1F
Reaction #91206
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1cc(F)c(OCc2cccnc2SC2CCC2)c(F)c1
Reaction #91213
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1ncccc1COc1c(F)cc(CC(C)C(=O)O)cc1F
Reaction #91220
title compound
Ausbeute 69.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1ccc(CC(C)(C)C(=O)O)cc1
Reaction #91226
title compound
Ausbeute 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1ccc(CCC(=O)O)cc1Cl
Reaction #91233
title compound
Ausbeute 101.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1ccc(C2CC2C(=O)O)cc1F
Reaction #91239
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1ccc(C2CC2C(=O)O)cc1Cl
Reaction #91250
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1ncccc1COc1ccc(C2CC2C(=O)O)cc1F
Reaction #91268
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1ncccc1COc1ccc(CCC(=O)O)cc1F
Reaction #91283
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1ccc(OCc2cccnc2SC2CCC2)c(F)c1
Reaction #91284
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1ccc(OCc2cccnc2SCC2CC2)c(F)c1
Reaction #91286
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter