Поиск подструктуры

1121458

CN(C)c1ccccc1CSC1=NC(=O)C(C)(C)N1
Reaction #3333
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C(C)(C)N=C1SCc1ccccc1N(C)C
Reaction #3336
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3341
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3342
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)NC(SCc2ccccc2)=NC1=S
Reaction #3347
2-benzylthio-5,5-dimethylimidazolin-4-thione
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccccc1CSC1=NC(SCc2ccccc2)=NC1(C)C
Reaction #3348
2-benzylthio-4-(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
CSC1=N[C@@H](c2cccc(F)c2)[C@@H](c2cccc(F)c2)N1.I
Reaction #46992
product 44
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1
CSC1=N[C@@H](c2ccccc2C)[C@@H](c2ccccc2C)N1.I
Reaction #46994
product 46
Выход 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CSC1=N[C@@H](c2cccc(C)c2)[C@@H](c2cccc(C)c2)N1.I
Reaction #46995
product 47
Выход 92.5%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1
Reaction #47002
product 122
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2ccccc2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47003
product 77
Выход 48.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCC2CCCCC2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47005
product 79
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1)C1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1C(=O)OC(C)(C)C
Reaction #47007
product 81
Выход 22.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2cc(F)c(F)c(F)c2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47009
product 83
Выход 67.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2ccc(F)cc2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47011
product 85
Выход 41.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2cccc(F)c2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47013
product 87
Выход 62.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2cc(F)cc(F)c2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47015
product 89
Выход 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCCc2ccccc2F)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47016
product 91
Выход 43.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCCc2ccccc2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47018
product 93
Выход 44.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccc(CSC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)cc1
Reaction #47028
product 197
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее