Recherche de Sous-structure

19811

COC(=O)CCc1ccc(C#N)cc1
Reaction #1687
colorless oil
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccccc1C(=O)NC1CN2CCC1CC2.Cl
Reaction #3858
N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide, hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Cc2cccc(OC)c2C1C(=O)OCC
Reaction #5441
desired product
Rendement 96.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1C(C#N)C(C#N)CC2
Reaction #5448
desired product
Rendement 85.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(S(=O)(=O)C[C@@H]2C[C@H](N)CC[C@@H]2NC(=O)OC(C)(C)C)cc1
Reaction #7775
(1S*,2R*,4R*)-[4-amino-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester
Rendement 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn2c(-c3ccc(OC)cc3Cl)cccc2c1[N+](=O)[O-]
Reaction #9281
title compound
Rendement 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn2c(-c3c(C)cc(C)cc3OC)ccc(OC)c2c1[N+](=O)[O-]
Reaction #9287
title compound
Rendement 98.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn2c(-c3c(C)cc(OC)cc3OC)cccc2c1N(CC1CC1)CC1CCOC1
Reaction #9298
title compound
Rendement 49.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(NC(=O)OC(C)(C)C)c(SC)nn12
Reaction #9303
title compound
Rendement 102.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c(-c2cccc3c(NC(=O)OC(C)(C)C)c(OC)nn23)c(OC)c1
Reaction #9322
title compound
Rendement 63.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CO)cc1
Reaction #44329
4-cyanobenzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(-c2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCNC3)c(Cl)c1
Reaction #51547
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncsc1CCC(=O)C(C)C
Reaction #51723
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1Oc2ccc(C(C)C(=O)OC)cc2C(=O)C1C
Reaction #54964
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCP(=O)([O-])[O-].[Ba+2]
Reaction #56113
white powder
Rendement 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(-c2ccsc2-c2ccnc3[nH]ccc23)cc1
Reaction #57215
title compound
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)ONS(=O)(=O)c1cccc(N)c1
Reaction #57424
product
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(-c2nn(C(c3ccccc3)(c3ccccc3)c3ccccc3)c3ccncc23)c1
Reaction #62363
title compound
Rendement 93.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)n1cc(-c2cc3c(/C=C/c4ccc(F)cc4)nn(C(C)=O)c3cc2F)cn1
Reaction #62410
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #62764
gum
DOI: 10.6084/m9.figshare.5104873.v1
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