部分構造検索

C(C#N)Cl

N#CCN1CCC(c2ccc(Oc3ccccc3)cc2)CC1
Reaction #1062
compound ( 26 )
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]cc(SCC#N)c2c1
Reaction #4408
5-methoxy-3-cyanomethylthioindole
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC#N)(Cc1cccc2ccccc12)C(=O)OCC
Reaction #4685
cyanomethyl-(α-naphthylmethyl)-malonic acid diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@H](OC(=N)C(Cl)(Cl)Cl)SC[C@H]1OC(C)=O
Reaction #6127
expected product
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C#N)c(C)c1C(C)=O
Reaction #6944
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N#CCN1CCN(Cc2ccccc2)CC1
Reaction #7694
N-benzyl-N′-cyanomethylpiperazine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=N)C(Cl)(Cl)Cl)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40596
21
収率 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(CC#N)CC1
Reaction #44339
4-Cyanomethyl-piperazine-1-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N#CCOc1ccccc1F
Reaction #47077
product 384
収率 97.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CCOc1cccc(F)c1
Reaction #47078
product 386
収率 94.2%DOI: 10.6084/m9.figshare.5104873.v1
N#CCOc1ccc(F)cc1
Reaction #47079
product 388
収率 95.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1OC12CCOCC2
Reaction #48663
desired compound
収率 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1ccc(N)n1
Reaction #48818
title compound
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2cccc3c2C(=O)OC3OCC#N)n1
Reaction #50444
3-cyanomethoxy-7-[(4,6-dimethoxy-pyrimidin-2-yl)oxy]-phthalide
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(Cl)Sc1cccc(Cl)c1
Reaction #50577
2,3-dichloro-phenylthioacetonitrile
収率 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1cc(CCC#N)ccc1-c1ccc(-c2ccc(OCC#N)c(Cc3ccccc3)c2)c(Cc2ccccc2)c1
Reaction #54110
29
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2cccc(C(F)(F)F)c2)c2ccc(OCC#N)cc2O1
Reaction #54573
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCOC(=O)c1cccnc1SCC#N
Reaction #55511
cyanomethyl 2-(cyanomethylthio)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1)c1cc2cc(Cl)ccc2s1
Reaction #56208
α-cyano-3-phenoxybenzyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CN(Cc2ccccc2)CCO1
Reaction #58590
title compound
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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