Recherche de Sous-structure

CC(C(C)O)O

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](Sc2cccc(C#N)c2)SC[C@H]1OC(C)=O
Reaction #6098
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2cccc(C#N)c2)SC[C@H]1OC(C)=O
Reaction #6099
expected product
Rendement 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2C#N)SC[C@H]1OC(C)=O
Reaction #6101
expected product
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2C#N)SC[C@H]1OC(C)=O
Reaction #6102
expected product
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2)SC[C@H]1OC(C)=O
Reaction #6105
expected product
Rendement 52.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2)SC[C@H]1OC(C)=O
Reaction #6106
expected product
Rendement 32.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(S[C@@H]2SC[C@@H](O)[C@H](O)[C@H]2O)cc1
Reaction #6121
expected product
Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O[C@@H]2CN[C@H]3[C@@H]2OC[C@@H]3O)cc1
Reaction #44472
(3R,3aR,6R,6aS)-3-hydroxyhexahydro-2H-furo[3,2-b]pyrrol-6-yl 4-methylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)NCCCO[C@@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O
Reaction #162037
white solid
Rendement 99.7%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1[C@H](O)CCC[C@@H]1Nc1nc(Cl)ncc1F
Reaction #162128
compound 31b
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(NC4(O)CCCCC4O)n3)c3cc(Cl)cnc32)cc1
Reaction #162129
compound 31c
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1C(OCc2ccccc2)OC(COCc2ccccc2)C(OC2OC(COCc3ccccc3)C(OCc3ccccc3)C(OCc3ccccc3)C2NC(C)=O)C1O
Reaction #173165
DOI: 10.1039/C8SC04228D
CC1CC(=O)NN=C1c1ccc(NC(=O)CCNCC(O)COc2ccc(CCOCC3CC3)cc2)cc1
Reaction #174428
DOI: 10.1039/C8SC04228D
COC(=O)C1OC1C1CC1
Reaction #181868
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(-c2cc(F)c(S(N)(=O)=O)cc2F)cc1)C(O)CCc1cccnc1
Reaction #187954
DOI: 10.1039/C8SC04228D
Nc1nc(C#CC2CCCCC2)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #189708
DOI: 10.1039/C8SC04228D
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