Ähnlichkeitssuche

11593

COc1cc(CC(=O)Oc2c(F)c(F)c(F)c(F)c2F)ccc1O
Reaction #7150
4-hydroxy-3-methoxyphenylacetic acid pentafluorophenyl ester
Ausbeute 98.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)Nc2cccc(C(=O)NC3CCCCC3)c2)ccc1O
Reaction #7166
desired compound
Ausbeute 94.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCN1C(=O)c2ccccc2C1=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #49183
Compound 43a
Ausbeute 101.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@H](Cc1ccc(C#N)cc1)NC(=O)OC(C)(C)C
Reaction #64405
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCc1c(OC)cccc1C(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #67912
pentafluorophenyl 2-allyloxymethyl-3-methoxybenzoate
Ausbeute 110.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3nc(Oc4c(F)c(F)c(F)c(F)c4F)ncc3C#N)c3cc(C(F)(F)F)cnc32)cc1
Reaction #69121
title compound
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Oc2c(F)c(F)c(F)c(F)c2F)ccc1Oc1ccccc1-c1ccccc1
Reaction #74566
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)c1ccc(OCc2ccccc2)cc1)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #81361
N-(4-(phenylmethoxy)benzoyl)glycine pentafluorophenyl ester
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #81364
N-(1,1-dimethylethoxycarbonyl)phenylalanine pentafluorophenyl ester
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)NCCc1ccccc1
Reaction #83118
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1c[nH]cn1
Reaction #83134
product
Ausbeute 47.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #84050
Pentafluorophenyl (1-azabicyclo[2.2.2]oct-3-yl)acetate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(=O)N1Cc1ccnc(Nc2ccccc2)n1
Reaction #184738
DOI: 10.1039/C8SC04228D
O=S(=O)(Oc1c(F)c(F)c(F)c(F)c1F)c1ccc(OCc2ccccc2)cc1
Reaction #217614
title compound ( D49 )
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2c(C(=O)Oc3c(F)c(F)c(F)c(F)c3F)cnc3ccc(C#N)cc23)cc1Cl
Reaction #218728
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCc1c(OC)cccc1C(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #221787
DOI: 10.1039/C8SC04228D
COc1ccc(CNc2c(C(=O)Oc3c(F)c(F)c(F)c(F)c3F)cnc3ccc(C#N)cc23)cc1Cl
Reaction #227571
DOI: 10.1039/C8SC04228D
CC(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #234706
DOI: 10.1039/C8SC04228D
N#CC(=Cc1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #234773
DOI: 10.1039/C8SC04228D
CCCCCOc1ccc(-c2ccc(-c3ccc(C(=O)Oc4c(F)c(F)c(F)c(F)c4F)cc3)cc2)cc1
Reaction #240878
DOI: 10.1039/C8SC04228D
Seite 1Weiter