Поиск подструктуры

6265

CN(CCO)C(C#N)c1ccc(Cl)c(Cl)c1
Reaction #1934
expected product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCC=C2C#N
Reaction #6483
title compound
Выход 60.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncccc1F
Reaction #7246
title compound
Выход 77.3%DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(-c2nc3ccccc3o2)cc1C(F)(F)F
Reaction #7790
[4-(1,3-benzoxazol-2-yl)-2-(trifluoromethyl)phenyl]acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(C#N)(CCl)OCCO
Reaction #56654
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)NC1(C#N)CCN(N(C)C)CC1
Reaction #72411
1-Dimethylamino-4-(N′,N′-dimethyl-hydrazino)-piperidine-4-carbonitrile
Выход 81.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1c2ccccc2C(Nc2ccc(Cl)cc2)=NN1C(=O)c1ccccc1
Reaction #78190
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)(C#N)c1ccc(Oc2ccccc2)cc1
Reaction #79493
2-chloro-2-(4-phenoxyphenyl)propionitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc(C#N)c1
Reaction #80631
2-cyano-4-methyl pyridine
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC=C(O[Si](C)(C)C)c2cc(C#Cc3ccc(C(=O)O)cc3)ccc21
Reaction #81669
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(c1ccccc1)CC2(O)CN
Reaction #82400
title compound
Выход 73.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(C1CCCCC1)CC2(O)CN
Reaction #82409
1-aminomethyl-5,6-dimethoxy-1-hydroxy-3-cyclohexyl-1,2,3,4-tetrahydronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(c1ccccc1)C=C2C#N
Reaction #82420
title compound
Выход 83.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(c1ccc(N2CCOCC2)cc1)C(O)C#N
Reaction #84858
2-hydroxy-3-methoxy-3-(4-morpholinophenyl)propanenitrile
Выход 94.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncccc1Cl
Reaction #85431
compound 145-C
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Br)c(C#N)n1
Reaction #89280
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1N1CCN(C3(C#N)CCCCC3)CC1)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #90148
title compound
Выход 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCCC2(O)CN
Reaction #91353
1-(aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol
Выход 68.4%DOI: 10.6084/m9.figshare.5104873.v1
NCC1(O)CCCc2cc(Br)ccc21
Reaction #91892
1-(aminomethyl)-6-bromo-1,2,3,4-tetrahydronaphthalen-1-ol
Выход 79.9%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1=CCCc2cc(Br)ccc21
Reaction #91894
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее