Substructure Search

5817

CS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)C3CCC2C3)c(Cl)c1Cl
Reaction #52573
2,3-Dichloro-4-methanesulfonylbenzoic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
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
CC12C=C(CCC(=O)CSc3ccccc3)C=CC1CC(=O)NC2=O
Reaction #82152
2-methyl-4-(3'-oxo-4'-phenylthiobutyl)-homophthalimide
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
CC(C)c1nc(CCOC2=CCC(C(C)(C)C)CC2)n(C)c1Sc1cc(Cl)cc(Cl)c1
Reaction #178300
DOI: 10.1039/C8SC04228D
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