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79615

Cc1ccccc1-c1ccc(Br)cn1
Reaction #231535
DOI: 10.1039/C8SC04228D
Cc1ccccc1-c1ccc(Br)cn1
Reaction #285385
DOI: 10.1039/C8SC04228D
Cc1ccccc1-c1ccc(Br)cn1
Reaction #580573
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(CO)cn1
Reaction #580575
product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1ccccc1-c1ccc(CBr)cn1
Reaction #580576
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(C[C@H](N=C(c2ccccc2)c2ccccc2)C(=O)OC(C)(C)C)cn1
Reaction #580577
(2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)C(Cc1ccc(-c2ccccc2C#N)nc1)C(=O)OC
Reaction #716222
methyl 2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxoheptanoate
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)C(Cc1ccc(-c2ccccc2C#N)nc1)C(=O)OC
Reaction #716226
methyl 2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxohexanoate
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(CC(N=C(c2ccccc2)c2ccccc2)C(=O)OC(C)(C)C)cn1
Reaction #901621
DOI: 10.1039/C8SC04228D
CCCCC(=O)C(Cc1ccc(-c2ccccc2C#N)nc1)C(=O)OC
Reaction #1710156
methyl 2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxoheptanoate
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(Br)cn1
Reaction #2307434
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(CO)cn1
Reaction #2307436
product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1ccccc1-c1ccc(CBr)cn1
Reaction #2307437
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(C[C@H](N=C(c2ccccc2)c2ccccc2)C(=O)OC(C)(C)C)cn1
Reaction #2307438
(2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(CO)cn1
Reaction #2420755
DOI: 10.1039/C8SC04228D
Cc1ccccc1-c1ccc(Br)cn1
Reaction #2509547
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(CO)cn1
Reaction #2509549
product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1ccccc1-c1ccc(CBr)cn1
Reaction #2509550
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccc(C[C@H](N=C(c2ccccc2)c2ccccc2)C(=O)OC(C)(C)C)cn1
Reaction #2509551
(2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1