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COc1cccc(C2(CCC#N)CCCC(=[N+]=[N-])C2=O)c1
Reaction #291255
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCC1(c2cccc(OC)c2)CCCCC1=O
Reaction #500607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCCCC(=O)O)CCCCC2=O)c1
Reaction #500608
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC(=O)N=[N+]=[N-])CCCCC2=O)c1
Reaction #524358
2-(β-Azidoformylethyl)-2-(m-methoxyphenyl)cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC#N)C=CCCC2)c1
Reaction #631450
1-(m-methoxyphenyl)-2-cyclohexene-1-propionitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC(=O)N=[N+]=[N-])CCCCC2=O)c1
Reaction #768966
DOI: 10.1039/C8SC04228D
COc1cccc(C2(CCC(=O)N=[N+]=[N-])CCCCC2=O)c1
Reaction #953721
2-(β-Azidoformylethyl)-2-(m-methoxyphenyl)cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC(=O)N=[N+]=[N-])CCCCC2=O)c1
Reaction #1046626
DOI: 10.1039/C8SC04228D
COc1cccc(C2(CCC#N)CCCC(C=O)C2=O)c1
Reaction #1212966
DOI: 10.1039/C8SC04228D
COc1cccc(C2(CCC#N)C=CCCC2)c1
Reaction #1243724
1-(m-methoxyphenyl)-2-cyclohexene-1-propionitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(c2cccc(OC)c2)CCCCC1=O
Reaction #1303668
DOI: 10.1039/C8SC04228D
COc1cccc(C2(CCC#N)CCCC(C=O)C2=O)c1
Reaction #1478428
2-(3-methoxyphenyl)-2-(2-cyanoethyl)-6-formylcyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC#N)CCCC(=[N+]=[N-])C2=O)c1
Reaction #1478429
2-(3-methoxyphenyl)-2-(2-cyanoethyl)-6-diazocyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC(=O)N=[N+]=[N-])CCCCC2=O)c1
Reaction #1501525
2-(β-Azidoformylethyl)-2-(m-methoxyphenyl)cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC(=O)N=[N+]=[N-])CCCCC2=O)c1
Reaction #1501528
2-(β-Azidoformylethyl)-2-(m-methoxyphenyl)cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(CCC(=O)N=[N+]=[N-])CCCCC2=O)c1
Reaction #1793980
2-(β-Azidoformylethyl)-2-(m-methoxyphenyl)cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(c2cccc(OC)c2)CCCC(Br)C1=O
Reaction #2163170
crude title compound
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(c2cccc(OC)c2)CCCc2sc(Nc3ccc(-n4cnc(C)c4)c(OC)c3)nc21
Reaction #2163171
title compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(c2cccc(OC)c2)CCCCC1=O
Reaction #2163226
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(c2cccc(OC)c2)CCCC(=CN(C)C)C1=O
Reaction #2163227
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
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