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Fc1ccc(Br)cc1F

CCCC1CCC(c2ccc(-c3ccc(F)c(F)c3)cc2)CC1
Reaction #1277
white crystals
Выход 94.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(-c2ccsc2)cc(F)c1F
Reaction #3169
3(3,4,5-trifluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccsc2)cc1F
Reaction #3170
3(3,4-difluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(F)cc(-c2ccsc2)c1
Reaction #3171
3(3,5-difluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccsc2)c(F)c1
Reaction #3172
pure product
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(C#Cc2cc(F)c(F)c(F)c2)cc1
Reaction #4969
3,4,5-trifluoro-4'-butoxytolan
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(F)c(F)c(Cl)c1NC1CC1
Reaction #10398
title compound
Выход 63.7%DOI: 10.6084/m9.figshare.5104873.v1
CCO[Si](OCC)(c1c(F)c(F)c(F)c(F)c1F)c1c(F)c(F)c(F)c(F)c1F
Reaction #12073
di(pentafluorophenyl)diethoxysilane
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/c1cc(F)c(F)c(F)c1
Reaction #44599
title compound
Выход 84.1%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
C/C=C/c1cc(F)c(F)c(F)c1
Reaction #44631
title compound
Выход 84.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc2c(cc1F)C1C=CC2O1
Reaction #57065
24
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)c(F)c1C(=O)c1ccc(Cl)nc1N
Reaction #58414
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)c1c(Br)ccc(F)c1F
Reaction #62298
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)c1c(Br)cc(C=O)c(F)c1F
Reaction #62299
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(Br)cc(F)c1F
Reaction #62300
title compound
Выход 75.6%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)c(F)c(C=O)c1
Reaction #62301
title compound
Выход 42.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)cc(N2CCOCC2)c1F
Reaction #69030
4-(5-bromo-2,3-difluorophenyl)morpholine
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nn1c2c(c3c(F)c(F)ccc31)CCC2.O=C(O)/C=C/C(=O)O
Reaction #77702
product
Выход 238.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(c2ccc(F)c(F)c2C(F)(F)F)CC1
Reaction #86696
tert-butyl 4-(3,4-difluoro-2-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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