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FCCCCCc1cccc(Br)c1

FCCCCCc1cccc(Br)c1
Reaction #58859
1-bromo-3-(5-fluoropentyl)benzene
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc([C@]23CO[C@@H](CF)C[C@H]2CSC(NC(=O)c2ccccc2)=N3)c(F)cc1F
Reaction #155581
N-[(4aR,6R,8aS)-8a-(5-cyano-2,4-difluorophenyl)-6-(fluoromethyl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
FCCC1CC(c2cccc(Br)c2)C1
Reaction #195792
DOI: 10.1039/C8SC04228D
CC1=NC2(N=C1N)c1cc(N)ccc1CC21CCC(F)(F)CC1
Reaction #271395
DOI: 10.1039/C8SC04228D
O=C1Nc2ccc(Br)cc2C2CCCC12F
Reaction #298873
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1=N[C@@]2(c3cc(Br)ccc3F)CO[C@@H](CF)C[C@H]2CS1
Reaction #305179
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cc(-c4cccnc4F)ccc3F)CO[C@@H](C(F)(F)F)C[C@H]2CS1
Reaction #305189
title compound
Ausbeute 14.5%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cc(-c4cccnc4F)ccc3F)CO[C@@H](CF)C[C@H]2CS1
Reaction #305190
title compound
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1
N=C1c2cc(Br)ccc2CC12CCC(F)(F)CC2
Reaction #373485
DOI: 10.1039/C8SC04228D
CC1=NC2(N=C1N)c1cc(Br)ccc1CC21CCC(F)(F)CC1
Reaction #392663
DOI: 10.1039/C8SC04228D
CC(C)[Si](C#Cc1cccc(C2CC(CCF)C2)c1)(C(C)C)C(C)C
Reaction #392911
DOI: 10.1039/C8SC04228D
N#Cc1cccc(-c2ccc3c(c2)C(=O)C2(CCC(F)(F)CC2)C3)c1
Reaction #560148
3-(4,4-difluoro-1′-oxo-1′,3′-dihydrospiro[cyclohexane-1,2′-indene]-6′-yl)benzonitrile
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC2(CC1)Cc1ccc(Br)cc1C2=O
Reaction #560186
compound 4
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)S(=O)N=C1c2cc(Br)ccc2CC12CCC(F)(F)CC2
Reaction #626522
title compound
Ausbeute 31.3%DOI: 10.6084/m9.figshare.5104873.v1
N=C1c2cc(Br)ccc2CC12CCC(F)(F)CC2
Reaction #626523
6′-bromo-4,4-difluorospiro[cyclohexane-1,2′-inden]-1′(3′H)-imine
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=NC2(NC1=S)c1cc(Br)ccc1CC21CCC(F)(F)CC1
Reaction #626524
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=NC2(N=C1N)c1cc(Br)ccc1CC21CCC(F)(F)CC1
Reaction #626525
title compound
Ausbeute 39.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1=NC2(N=C1N)c1cc(-c3cncc(Cl)c3)ccc1CC21CCC(F)(F)CC1
Reaction #626526
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=NC2(N=C1N)c1cc(N)ccc1CC21CCC(F)(F)CC1
Reaction #626527
title compound
Ausbeute 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC#Cc1cncc(-c2ccc3c(c2)C2(N=C(C)C(N)=N2)C2(CCC(F)(F)CC2)C3)c1
Reaction #626529
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
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