Поиск подструктуры

14150026

Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #132
Выход 54.9%
Clc1ccnc(Nc2ncco2)c1
Reaction #415
Выход 0.5%
Clc1ccnc(Nc2ncco2)c1
Reaction #459
Выход 3.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #462
Выход 2.5%
Cc1c(I)ccc2c1C(=O)NS2(=O)=O
Reaction #906
iodine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=NO)C(=NO)C[C@]4(C)[C@H]3CC[C@]12C
Reaction #928
17β-Acetoxy-2,3-dihydroxyimino-5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C(=O)O)c2c1CCCC2
Reaction #1178
hydrazine
Выход 73.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NN)ccc(C(=O)O)c1C.Cl
Reaction #1179
expected product
Выход 93.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)ccc1NN.Cl
Reaction #1180
4-Hydrazino-3-methoxybenzoic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc(NN)cc1Cl
Reaction #1181
2-Chloro-4-hydrazinobenzonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(Cl)c(C(=O)O)c1
Reaction #1182
expected product
Выход 123.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)O)cc1NN.Cl
Reaction #1183
3-Hydrazino-4-methylbenzoic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)O)ccc1I
Reaction #1232
3-methyl-4-iodobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(=NO)C(=O)c1c(C)cc(C)cc1C
Reaction #1249
semi-solid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H](Br)Cc1ccccc1
Reaction #1285
(S)-α-Bromobenzenepropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@H](Br)C(=O)O
Reaction #1291
crude title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)c(F)cc(F)c1C#N
Reaction #1368
2-methyl-3,4,6-trifluorobenzonitrile
Выход 38.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H](Br)Cc1ccccc1
Reaction #1419
(S)-α-Bromobenzenepropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@H](Br)C(=O)O
Reaction #1425
crude title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](Br)C(=O)O
Reaction #1427
crude title product
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее