Teilstruktursuche

O=Cc1cc(F)cc(F)c1

O=C(Cl)c1cc(F)c(F)c(F)c1F
Reaction #3055
2,3,4,5-tetrafluorobenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC=C(C#N)C(=O)c1cc(F)c(F)c(F)c1F
Reaction #4362
2-(2,3,4,5-tetrafluorobenzoyl)-3-methoxy-acrylonitrile
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(=O)c1cc(F)c(OC)c(F)c1
Reaction #7334
Methyl (3,5-difluoro-4-methoxybenzoyl)acetate
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(F)c(F)c1F
Reaction #10364
title compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1c(F)c(F)c(F)c(F)c1F
Reaction #10367
title compound
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(F)c1F
Reaction #10375
title compound
Ausbeute 74.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1cc(F)cc(F)c1
Reaction #10885
2-bromo-1-(3,5-difluorophenyl)ethanone
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1c(F)c(F)c(-c2nnc(-c3cc(Cl)ccc3Cl)o2)c(F)c1F
Reaction #11276
2-(2,5-dichlorophenyl)-5-(pentafluorophenyl)-1,3,4-oxadiazole
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](COCC(=O)c1cc(F)c(F)c(F)c1)COCc1ccccc1
Reaction #44625
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1
Reaction #44626
title compound
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #46477
Compound 151
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC[C@H](NC(=O)c1cc(F)c(F)c(F)c1F)C(=O)OC(C)(C)C
Reaction #51888
di-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)c1cc(F)c(C)c(F)c1Cl
Reaction #62851
diethyl 2-chloro-3,5-difluoro-4-methylbenzoyl-malonate
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)cc(C(=O)Cl)c(Cl)c1F
Reaction #62867
3,5-difluoro-4-methyl-6-chlorobenzoyl chloride
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1
OCc1c(F)c(F)c(Br)c(F)c1F
Reaction #62878
4-bromo-2,3,5,6-tetrafluorobenzyl alcohol
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1
NCCN.O=C(O)c1c(F)c(F)c(F)c(F)c1F.O=C(O)c1c(F)c(F)c(F)c(F)c1F
Reaction #68736
ethylene diamine bis(pentafluorobenzoate)
DOI: 10.6084/m9.figshare.5104873.v1
NCCN.[N-]=[N+]=Nc1c(F)c(F)c(C(=O)O)c(F)c1F.[N-]=[N+]=Nc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #68737
ethylene diamine bis(4-azido-2,3,5,6-tetrafluorobenzoate)
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(F)cc(C(=O)O)cc1F
Reaction #69374
title compound
Ausbeute 35.6%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(F)c(C=O)c(F)c1
Reaction #69375
title compound
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)nc(-c1c(F)cc(C(=O)O)cc1F)n2C[C@@H]1CN(C(=O)OC(C)(C)C)CCO1
Reaction #69382
(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid
Ausbeute 82.3%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter