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25667

COC(=O)C(CC=CCBr)CC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O
Reaction #61230
2-(4-bromo-but-2-enyl)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-4-methyl-hex-4-enoic acid methyl ester
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC=CCBr)CC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O
Reaction #61894
2-(4-bromo-but-2-enyl)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-4-methyl-hex-4-enoic acid methyl ester
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C/C=C/CBr
Reaction #64859
title product
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(O)c2c1C1(Br)C(Br)=C(Br)C2(Br)C1(Br)Br
Reaction #74967
1,2,3,4,9,9-hexabromo-1,4-dihydro-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OCC=CCBr)c([N+](=O)[O-])c1
Reaction #78797
1-bromo-4-(2,4-dinitrophenyloxy)but-2-ene
Ausbeute 46.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc([N+](=O)[O-])c(OCC=CCBr)c1
Reaction #78798
1-bromo-4-(2,5-dinitrophenyloxy)but-2-ene
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)c1cccc(OCC=CCBr)c1
Reaction #78799
1-bromo-4-[3-(perfluoro-n-octyl)phenoxy]but-2-ene
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CC=CCBr
Reaction #180332
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(OCC=CCBr)c([N+](=O)[O-])c1
Reaction #194821
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CC=CCBr
Reaction #231081
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)N2CC3=C(CN(C)C3)C2)cc1
Reaction #231097
DOI: 10.1039/C8SC04228D
NS(=O)(=O)c1cc(C(=O)O)cc(NCC=CCBr)c1Oc1ccccc1
Reaction #236569
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CC=CCBr
Reaction #269232
DOI: 10.1039/C8SC04228D
CCOP(=O)(CC=CCBr)OCC
Reaction #269554
DOI: 10.1039/C8SC04228D
COC(=O)C(CC=CCBr)CC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O
Reaction #359309
2-(4-bromo-but-2-enyl)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-4-methyl-hex-4-enoic acid methyl ester
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC=CCBr)CC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O
Reaction #359326
2-(4-bromo-but-2-enyl)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-4-methyl-hex-4-enoic acid methyl ester
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
C(=CCN(c1ccccc1)c1ccccc1)CN(c1ccccc1)c1ccccc1
Reaction #362394
title compound
Ausbeute 39.3%DOI: 10.6084/m9.figshare.5104873.v1
C(=CCN(c1ccccc1)c1cccc2ccccc12)CN(c1ccccc1)c1cccc2ccccc12
Reaction #362395
title compound
Ausbeute 17.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C#N)C=CC(C)(C#N)C=C1
Reaction #366606
1,4-dicyano-p-xylene
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OCC=CCOc2ccc([N+](=O)[O-])cc2)cc1
Reaction #367323
1,4-Bis-(4-nitrophenoxy)-2-butene
DOI: 10.6084/m9.figshare.5104873.v1
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