Поиск подструктуры

C=CBr

COC(=O)c1cncn1C1c2ccccc2C(Br)=CC1(C)C
Reaction #5870
1-(2,2-dimethyl-4-bromo-1,2-dihydronaphthalin-1-yl)-5-imidazolecarboxylic acid methyl ester
Выход 51.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(Br)C1C(=O)OC
Reaction #6070
title compound
Выход 19.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C(C)CCC1O
Reaction #9397
2-ethyl-3-methyl-cyclopent-2-enol
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(N)=O)c(C)c(I)c1Br
Reaction #45571
compound
Выход 50.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C(C)CCC1O
Reaction #57037
2-ethyl-3-methyl-cyclopent-2-enol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=C(Br)c2cc3c(cc2C1)OCO3
Reaction #62987
2-n-butyl-3-bromo-5,6-methylenedioxyindene
Выход 68.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=C(N(CC)CC)c2cc3c(cc2C1)OCO3
Reaction #62991
2-n-butyl-3-diethylamino-5,6-methylenedioxyindene
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(C2=C(Br)CCC2)cc1
Reaction #65796
1-(2-bromocyclopenten-1-yl)-4-(methylthio)benzene
Выход 32.6%DOI: 10.6084/m9.figshare.5104873.v1
BrC1=C(c2ccccc2)CCC1
Reaction #65804
1-bromo-2-phenylcyclopentene
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=CC(C)N1CCOCC1
Reaction #75079
N-oct-3-en-2-ylmorpholine
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75081
mixture
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC=CC(C)N1CCOCC1
Reaction #75082
6-morpholino-1,4-heptadiene
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC=CCC=C(C)CN1CCOCC1
Reaction #75083
2-methyl-1-morpholino-2,5-heptadiene
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccc(Cl)cc1)N1CCCc2cc(OCC=CCBr)ccc21
Reaction #77745
6-(4-Bromo-but-2-enyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid 4-chloro-phenyl ester
Выход 57.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2cc(OCC=CCBr)ccc21
Reaction #77750
6-(4-Bromo-but-2-enyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2cc(OCC=CCBr)ccc21
Reaction #77771
5-(4-Bromo-but-2-enyloxy)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
Выход 31.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1C2=C([N+](=O)[O-])C=C(Br)CC2CCC1CC(=O)OC
Reaction #80761
title compound
Выход 106.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80762
title compound
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[SH]1C(Br)=C(C=O)c2c1n(C)c(=O)n(CCCOC1CCCCO1)c2=O
Reaction #92181
ethyl 6-bromo-1-methyl-2,4-dioxo-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)-1,2,3,4-tetrahydro thieno[2,3-d]pyrimidine-5-carbaldehyde
Выход 57.5%DOI: 10.6084/m9.figshare.5104873.v1
NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=C(Br)Br)CS[C@H]12
Reaction #93028
benzhydryl 7-amino-3-(2,2-dibromovinyl)-3-cephem-4-carboxylate
Выход 82.6%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее