Substructure Search

C=CCC

Cc1ccc(C2=CC(C)(C)Sc3ccc(Br)cc32)cc1
Reaction #2710
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2=CC(C)(C)Sc3ccc(C=O)cc32)cc1
Reaction #2711
2,2-Dimethyl-4(tol-4-yl)-thiochrom-3-en-6-al
DOI: 10.6084/m9.figshare.5104873.v1
CC(=CC(=O)c1ccc(C(F)(F)F)cc1)N(C)C
Reaction #9733
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cccs2)ccc1C(=O)/C=C/c1ccc(C(=O)O)cc1
Reaction #10722
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10750
title compound
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cccs2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10757
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1[nH]c(C(C)(C)C)cc1N
Reaction #47203
methyl 3-amino-5-tert-butyl-1H-pyrrole-2-carboxylate
Yield 34.0%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
CCCCc1ncc(/C=C(\Cc2cccs2)C(N)=O)n1Cc1ccccc1[N+](=O)[O-]
Reaction #65285
title compound
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
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