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838029

CCN(CC=CC#CC(C)(C)C)Cc1cccc(OCc2cccc(-n3cccc3)c2)c1
Reaction #372352
DOI: 10.1039/C8SC04228D
BrCc1cccc(Oc2ccccc2)c1
Reaction #456558
3-phenoxybenzyl bromide
DOI: 10.6084/m9.figshare.5104873.v1
CCN(C/C=C/C#CC(C)(C)C)Cc1cccc(O)c1
Reaction #571717
(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-ethyl-3-hydroxybenzylamine
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C/C=C/C#CC(C)(C)C)Cc1cccc(O)c1
Reaction #571718
(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-propyl-3-hydroxybenzylamine
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C/C=C/C#CC(C)(C)C)Cc1cccc(OCc2cc(-c3ccsc3)cs2)c1
Reaction #571720
(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-ethyl-3-[4-(3-thienyl)-2-thienylmethyoxy]benzylamine
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C/C=C/C#CC(C)(C)C)Cc1cccc(O)c1
Reaction #574964
(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-ethyl-3-hydroxybenzylamine
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C/C=C/C#CC(C)(C)C)Cc1cccc(O)c1
Reaction #574966
(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-propyl-3-hydroxybenzylamine
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C/C=C/C#CC(C)(C)C)Cc1cccc(OCc2cccc(-c3ccsc3)c2)c1.Cl
Reaction #574971
(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-ethyl-3-(3-(3-thienyl)benzyloxy]benzylamine hydrochloride
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC=CC#CC(C)(C)C)Cc1cccc(OCC=CCn2ccnc2)c1
Reaction #768854
DOI: 10.1039/C8SC04228D
CCCN(CC=CC#CC(C)(C)C)Cc1cccc(O)c1
Reaction #773626
DOI: 10.1039/C8SC04228D
CCN(CC=CC#CC(C)(C)C)Cc1cccc(OCc2cccc(-c3ccsc3)c2)c1
Reaction #894570
DOI: 10.1039/C8SC04228D
CN(CC=CC#CC(C)(C)C)Cc1cccc(OCC=CCCl)c1
Reaction #909257
DOI: 10.1039/C8SC04228D
CN(CC=CC#CC(C)(C)C)Cc1cccc(O)c1
Reaction #1036496
DOI: 10.1039/C8SC04228D
CN(CC=CC#CC(C)(C)C)Cc1cccc(O)c1
Reaction #1208684
DOI: 10.1039/C8SC04228D
Cl
Reaction #1295063
DOI: 10.1039/C8SC04228D
CCN(C/C=C/C#CC(C)(C)C)Cc1cccc(OCC/C=C/c2ccsc2)c1
Reaction #1551926
(E,E)-N-ethyl-N-(6,6-dimethyl-2-hepten-4-ynyl)-3-[4-(3-thienyl)-3-butenyloxy]benzylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C/C=C/C#CC(C)(C)C)Cc1cccc(OC/C=C/Cn2ccnc2)c1
Reaction #1551927
captioned compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C/C=C/C#CC(C)(C)C)Cc1cccc(OC/C=C/CCl)c1
Reaction #1551933
captioned compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1
BrCc1cccc(Oc2ccccc2)c1
Reaction #1629992
DOI: 10.1039/C8SC04228D
CN(CC=CC#CC(C)(C)C)Cc1cccc(OCc2ccccc2)c1
Reaction #1632314
DOI: 10.1039/C8SC04228D
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