部分構造検索

1303568

O=C(O)[C@@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7125
product
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc(Cl)cc2)cc(-c2cc(Cl)ccc2OCC2CCCCC2)n1
Reaction #56931
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1(C(=O)O)CCCCC1)c1cc2ccccc2s1
Reaction #161036
title compound
収率 83.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(c2cc3ccccc3s2)=NC12CCCCC2
Reaction #161037
title compound
収率 76.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162181
racemic product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)CCCC(N=[N+]=[N-])C1O
Reaction #162206
racemic methyl-3-azido-2-hydroxy-1-methyl-cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C3CCCC(CO)C3)CC2)ccc1Cl)c1ccc(Cl)cc1Cl
Reaction #162318
desired product
収率 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1CC[C@H](C(F)(F)F)CC1
Reaction #168441
[trans-4-(trifluoromethyl)cyclohexyl]methanol
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CCC(c2nc(-c3cccc(OCc4c(F)cccc4F)c3)c3c(N)nccn23)CC1
Reaction #178176
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(COCC1CCCCC1)C(=O)O
Reaction #179430
DOI: 10.1039/C8SC04228D
NS(=O)(=O)CCCOc1cccc2c1ccn2-c1ccnc(NC2CCC(C(=O)O)CC2)n1
Reaction #180573
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)cc1)N(Cc1ccc(-c2ncco2)c(F)c1F)C1CCCCC1CO
Reaction #180670
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #187241
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OCC1CCC(Nc2cc(-c3cccc(NCc4cccc(F)c4)n3)c(Cl)cn2)CC1
Reaction #189787
DOI: 10.1039/C8SC04228D
O=C(O)C1(O)CCC(F)(F)CC1
Reaction #191170
DOI: 10.1039/C8SC04228D
COc1ccccc1C(C)C(=O)N1CC2CC(CC#N)CC(O)(c3ccccc3OC)C2C1
Reaction #194868
DOI: 10.1039/C8SC04228D
Nc1nccn2c(C3CCC(C(=O)O)CC3)nc(-c3ccc4ccc(-c5ccccc5)nc4c3)c12
Reaction #195624
DOI: 10.1039/C8SC04228D
CCNc1cc(S(=O)(=O)NC2CCC(C(=O)O)CC2)ccc1Cl
Reaction #204141
DOI: 10.1039/C8SC04228D
C=CCC1(C(=O)OCC)CCC(O)CC1
Reaction #212291
DOI: 10.1039/C8SC04228D
CCc1oc(-c2cccc(OC)c2)nc1COC1CCCC(COC(C)(C)C(=O)O)C1
Reaction #221829
DOI: 10.1039/C8SC04228D
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