Recherche de Sous-structure

8553

CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6088
expected product
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6089
expected product
Rendement 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6090
expected product
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(S[C@@H]2SC[C@@H](O)[C@H](O)[C@H]2O)cc1
Reaction #6091
expected product
Rendement 89.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2C#N)SC[C@H]1OC(C)=O
Reaction #6116
expected product
Rendement 40.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2C#N)SC[C@H]1OC(C)=O
Reaction #6117
expected product
Rendement 47.9%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(S[C@@H]2SC[C@@H](O)[C@H](O)[C@H]2O)c(C#N)c1
Reaction #6118
expected product
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C#N)c(S)c(C#N)c1
Reaction #6119
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2c(C#N)cc(C#N)cc2C#N)SC[C@H]1OC(C)=O
Reaction #6120
expected product
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(S(=O)(=O)CC2CN(CC(=O)c3ccc(F)cc3)C2)cc1
Reaction #10311
gum
Rendement 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC[n+]1ccccc1.N#Cc1ccc(S(=O)[O-])cc1
Reaction #43892
product
Rendement 108.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[n+]1c(C)oc2ccccc21.N#Cc1ccc(S(=O)[O-])cc1
Reaction #43893
product
Rendement 46.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc2c(cc1S)CCN2S(=O)(=O)c1ccc(C#N)cc1
Reaction #51759
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63567
solid
Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1S(=O)(=O)N1CCN[C@@H](C)C1
Reaction #69578
title compound
Rendement 108.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(S(=O)(=O)NC(C)(C)C)ccc1C#N
Reaction #70617
N-tert-butyl-4-cyano-3-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(S(=O)(=O)NC(C)(C)C)ccc1CN
Reaction #70618
4-(aminomethyl)-N-tert-butyl-3-methylbenzenesulfonamide
Rendement 113.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(S(=O)(=O)NC(C)(C)C)ccc1C(C)N
Reaction #70623
4-(1-aminoethyl)-N-tert-butyl-3-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1S(=O)(=O)N1CCN[C@@H](C)C1
Reaction #71649
title compound
Rendement 108.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1S(=O)(=O)N1CCNC[C@@H]1C
Reaction #71652
title compound
Rendement 91.5%DOI: 10.6084/m9.figshare.5104873.v1
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