Поиск подструктуры

3138

C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #202
Выход 35.7%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #204
Выход 31.5%
c1cncc(N2CCNCC2)c1
Reaction #216
Выход 0.0%
CC(=O)Nc1cnc(N2CCN(C)CC2)cn1
Reaction #299
Выход 79.5%
CC(C)(C)OC(=O)NCCC1CCN(c2ccccc2)CC1
Reaction #317
Выход 0.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #365
Выход 15.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #366
Выход 0.0%
COc1nc(Nc2ccc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #440
Выход 0.0%
COc1nc(Nc2ccc3c(n2)OC(CC(F)(F)F)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #506
Выход 50.0%
COc1nc(Nc2ccc3c(n2)OC(CC(F)(F)F)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #507
Выход 85.3%
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #597
Выход 2.3%
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #598
Выход 0.0%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(O)cc1
Reaction #760
Выход 0.0%
C[C@@H]1CN(c2ccc(S(C)(=O)=O)cc2)CCN1C(=O)OC(C)(C)C
Reaction #787
Выход 0.0%
FC1(F)Oc2ccc(N3CCNCC3)cc2O1
Reaction #802
Выход 50.7%
COc1ccc(N2CCN(C(=O)OC(C)(C)C)[C@H](C(C)C)C2)cc1OC
Reaction #813
Выход 90.5%
COC(=O)[C@H](Cc1ccccc1)n1cc(-c2cccc3ccccc23)cc(NC(=O)c2ccc(C(F)(F)F)cc2)c1=O
Reaction #7903
title compound
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc3[nH]ccc3c2)CC1
Reaction #8433
product
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)ccc1OCC(=O)O
Reaction #9436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3cccc(C(F)(F)F)c3)cc2)c2ccc(-c3cccc(C(F)(F)F)c3)cc2)ccc1OCC(=O)O
Reaction #9438
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее