부분 구조 검색

CC(C)=CBr

Cc1cc(C2C=CCC2)c(S(C)(=O)=O)cc1C(=O)N=C(N)N
Reaction #2988
N-diaminomethylene-2-methyl-4-(1-cyclopentene-3-yl)-5-methylsulfonylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1-c1ccc(CN2C(=O)c3ccccc3C2=O)cc1
Reaction #5957
title compound
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CC1(C)CCC(=O)C(Br)=C21
Reaction #7917
4-bromo-7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
수율 46.5%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(=O)C(Br)=C1c1ccc(O)cc1C2
Reaction #7918
4-bromo-7-hydroxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCC2(CCCC)Cc3cc(O)ccc3C2=C1Br
Reaction #7929
4-bromo-9a-butyl-3-methylene-2,3,9,9a-tetrahydro-1H-fluoren-7-ol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(Br)c2oc(C3CC3)nc2c1C#N
Reaction #45583
compound
수율 85.7%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46167
title compound
수율 83.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Br)=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc21
Reaction #47815
titled compound
수율 60.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #47816
titled compound
수율 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(-c2cc(C=C3C(=O)Nc4ccccc43)ccc2OC)c1
Reaction #52681
3-(3′-ethoxy-6-methoxy-biphenyl-3-ylmethylene)-1,3-dihydroindol-2-one
수율 397.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75081
mixture
수율 61.0%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
수율 57.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/Br)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157711
title compound
수율 25.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/N2CCCC2=O)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157882
1-[(E)-2-(4-tert-butylphenyl)-2-(5-chloro-6-methoxypyridin-2-yl)ethenyl]pyrrolidin-2-one
수율 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(Br)C=O)c1ccc2c(c1)C(C)(C)CCC2(C)C
Reaction #174038
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1cccc(C=C2c3ccccc3Oc3ccccc32)c1
Reaction #178518
DOI: 10.1039/C8SC04228D
CC12C=CC(=O)CC1C(=CBr)CCC2
Reaction #180132
DOI: 10.1039/C8SC04228D
COc1ccc(CN2C(=O)C(C)=C(c3ccc(C(F)(F)F)cc3)C2=O)c(OC)c1
Reaction #187137
DOI: 10.1039/C8SC04228D
COc1ncc(OC)c2c(C(=O)C(=O)N3CCC(=C(c4ccccc4)c4nccs4)CC3)c[nH]c12
Reaction #195061
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(C2=C(c3cc(C(F)(F)F)ccc3OCc3ccc(F)cc3)CCC2)ccc1N
Reaction #196847
DOI: 10.1039/C8SC04228D
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