部分構造検索

770703

Cl.Nc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #216144
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #216145
desired product
収率 114.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C[C@@H]2COC(=O)N2)cc1
Reaction #216159
desired product
収率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)OC[C@@H]1Cc1ccc(N)cc1.Cl
Reaction #216160
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)OC[C@@H]1Cc1ccc(NN)cc1.Cl
Reaction #216161
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC=C(c2c[nH]c3ccc([C@@H]4COC(=O)N4)cc23)CC1.O
Reaction #216164
(R)-3(1-Methyl-1,2,3,6-tetrahydro-4-pyridyl)-5-(2-oxo-1,3-oxazolidin-4-yl)-1H-indole hydrate
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCC=NNc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #216169
desired product
収率 93.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #431075
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #431076
desired product
収率 114.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #431089
solid
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)OC[C@@H]1Cc1ccc(N)cc1.Cl
Reaction #431090
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)OC[C@@H]1Cc1ccc(NN)cc1.Cl
Reaction #431091
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC=C(c2c[nH]c3ccc([C@@H]4COC(=O)N4)cc23)CC1.O
Reaction #431094
(R)-3-(1-Methyl-1,2,3,6-tetrahydro-4-pyridyl)-5-(2-oxo-1,3-oxazolidin-4-yl)-1H-indole hydrate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #1696155
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #1696156
desired product
収率 114.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C[C@@H]2COC(=O)N2)cc1
Reaction #1696170
desired product
収率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)OC[C@@H]1Cc1ccc(N)cc1.Cl
Reaction #1696171
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)OC[C@@H]1Cc1ccc(NN)cc1.Cl
Reaction #1696172
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC=C(c2c[nH]c3ccc([C@@H]4COC(=O)N4)cc23)CC1.O
Reaction #1696175
(R)-3-(1-Methyl-1,2,3,6-tetrahydro-4-pyridyl)-5-(2-oxo-1,3-oxazolidin-4-yl)-1H-indole hydrate
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCC=NNc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #1696180
desired product
収率 93.2%DOI: 10.6084/m9.figshare.5104873.v1