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1148097

C[SH](CC(N)=S)(c1ccc(F)cc1)(c1ccc(F)cc1)c1ccccc1F
Reaction #61885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCN(c1ccc(F)c(C(C)=O)c1F)S(=O)(=O)c1cc(F)ccc1F
Reaction #74174
N-(3-acetyl-2,4-difluoro-phenyl)-2,5-difluoro-N-(2-methoxy-ethoxymethyl)-benzene-sulfonamide
Ausbeute 62.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(n2nccc2-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ncns3)cc2F)C1
Reaction #74534
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]cc1-c1cc(C(F)(F)F)ccc1Oc1cc(F)c(S(=O)(=O)Nc2cscn2)cc1Cl
Reaction #74543
amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3cccnn3)cc2Cl)ccn1
Reaction #74546
product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]cc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2cccnn2)cc1Cl
Reaction #74552
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cccnn1)c1cc(Cl)c(F)cc1F
Reaction #74670
desired product
Ausbeute 24.9%DOI: 10.6084/m9.figshare.5104873.v1
CSc1c(F)cc(-c2cc(C(F)(F)F)nn2-c2ccc(F)cc2)cc1F
Reaction #75918
5-[3,5-difluoro-4-(methylthio)-phenyl]-1-(4-fluorophenyl)-3-(trifluoromethyl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
CSc1c(F)cc(CC(=NO)c2ccccc2)cc1F
Reaction #75927
2-[3,5-difluoro-4-(methylthio)phenyl]-1-phenylethanone oxime
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1c(F)cc(-c2c(-c3ccccc3)noc2C)cc1F
Reaction #75928
4-[3,5-difluoro-4-(methylthio)phenyl]-5-methyl-3-phenylisoxazole
Ausbeute 48.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C(F)(F)F)cc1S
Reaction #78234
4-fluoro-3-mercaptobenzotrifluoride
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)cc1F
Reaction #157528
title compound
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #157594
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)cc1F
Reaction #157597
title compound
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Cl)cc1NS(=O)(=O)c1cccc(Cl)c1F
Reaction #157598
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCS(=O)c1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)cc1F
Reaction #157654
title compound
Ausbeute 22.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(SC(F)(F)F)c(F)c1)c1cnc(Cl)c(Br)c1
Reaction #160948
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2cccc(S(C)(=O)=O)c2F)CC1
Reaction #178572
DOI: 10.1039/C8SC04228D
O=C1CCCN1c1cccc(SCc2ccccc2)c1F
Reaction #186303
DOI: 10.1039/C8SC04228D
N#CC(=Cc1cc(Sc2cccc(C3OCCCO3)c2)c(F)cc1[N+](=O)[O-])CC1CCOCC1
Reaction #190789
DOI: 10.1039/C8SC04228D
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