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C(C#N)Br

N=C(NC(=O)OCc1ccccc1)c1ccc(CN)cc1
Reaction #953
4-aminomethyl-1-(N-benzyloxycarbonylamidino)benzene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C=C2SCN(CC#N)C2=O)cc(C(C)(C)C)c1O
Reaction #3041
desired title product
Выход 40.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CCN1CCC(c2cccc3ccccc23)CC1
Reaction #5061
hydrochloride
Выход 91.8%DOI: 10.6084/m9.figshare.5104873.v1
N#CCN1CC=C(c2cccc3c2OCCO3)CC1
Reaction #5068
[4-(1,4-Benzodioxan-5-yl)-1,2,3,6-tetrahydropyrid-1-yl]acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7051
0.244-g
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(CC#N)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7404
title compound
Выход 27.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCCCC1)N1CC[C@H](N(CC#N)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7411
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(OCC#N)cccc12)NC(=O)OC(C)(C)C
Reaction #8192
[2-(7-cyanomethoxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester
Выход 86.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2c(OCC#N)cccc12)NC(=O)OC(C)(C)C
Reaction #8194
racemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester
Выход 70.2%DOI: 10.6084/m9.figshare.5104873.v1
N#CCOc1cccc2[nH]ccc12
Reaction #8215
(1H-indol-4-yloxy)acetonitrile
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCn1ccc2ccccc21
Reaction #8216
indol-1-yl-acetonitrile
Выход 27.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#Cc2cn(CC#N)c(C)n2)ccn1
Reaction #8963
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11685
title compound
Выход 26.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1OCC#N
Reaction #11798
title compound
Выход 102.8%DOI: 10.6084/m9.figshare.5104873.v1
N#CCCC(=O)c1cc(Cl)ccc1O
Reaction #11824
title compound
Выход 58.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=C(Br)C#N)CC1
Reaction #43780
title compound
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=C(C#N)CO)CC1
Reaction #43781
title compound
Выход 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3CC#N)CC1
Reaction #48124
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cn(CC#N)c2c(Cl)cccc12
Reaction #51670
(7-Chloro-3-methanesulfonyl-indol-1-yl)-acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#CCn1ccc2cc([N+](=O)[O-])ccc21
Reaction #51683
(5-Nitro-indol-1-yl)-acetonitrile
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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