Substructure Search

CCCC=C

C=CCCC1(C2=CCCC(C)(C)C2)OCCO1
Reaction #54161
1-(3,3-dimethyl-cyclohex-6-en-1-yl)-1,1-ethylenedioxy-pent-4-ene
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C=CCC(C)(C)C1
Reaction #54165
1-Methylene-3,3-dimethyl-cyclohex-5-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56547
beta-carotene
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56548
beta-carotene
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56549
beta-carotene
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56550
beta-carotene
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56554
beta-carotene
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56555
beta-carotene
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=C(c3cc(C)sc3C)CCC=C2)c(C)s1
Reaction #70957
25
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C\C=C\C(C)=C\C(=O)O)C(C)(C)CCC1
Reaction #71591
9-(Z)-retinoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)CC(C)O)C(C)(C)CC=C1
Reaction #74867
residue
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCC[Si](OCC)(OCC)OCC)C(N)=O
Reaction #83163
liquid
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162189
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162191
62a
Yield 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1(C[N+](=O)[O-])CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162192
62b
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(/C=C/[C@H]2CCCN2c2ncnc3[nH]cnc23)c1
Reaction #168581
6-[(R)-2-((E)-2-(3-chlorophenyl)vinyl)pyrrolidin-1-yl]-9H-purine
Yield 16.5%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(F)c(C2=CC(=O)CCC2)nc1Nc1ccc(N2CCOCC2)cc1
Reaction #174479
DOI: 10.1039/C8SC04228D
C=CCON=C(CCC)C1=C(O)CC(c2cc(C)cs2)CC1=O
Reaction #175365
DOI: 10.1039/C8SC04228D
Cl
Reaction #175811
DOI: 10.1039/C8SC04228D
CC(C)(C)C(O)C(=Cc1ccc(Cl)cc1)n1cncn1
Reaction #181908
DOI: 10.1039/C8SC04228D
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