部分構造検索

686641

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
収率 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
収率 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
収率 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
収率 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
収率 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
収率 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
収率 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
収率 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
収率 32.3%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc(S[C@@H]3SC[C@@H](O)[C@H](O)[C@H]3O)cc2)cc1
Reaction #6113
expected product
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)O)c1
Reaction #48776
desired compound
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)Nc2ccn(C(=O)OC(C)(C)C)n2)c1
Reaction #48780
title compound
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc2c(c1)OC(CNCCO)CO2
Reaction #67197
2-({[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}AMINO)ETHANOL
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(S(=O)(=O)NC(C(=O)O)C(OCc3ccccc3)C(O)CSc3nccs3)cc2)cc1
Reaction #174962
DOI: 10.1039/C8SC04228D
Nc1nc(C#CC2CCCCC2)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #189708
DOI: 10.1039/C8SC04228D
Nc1nc(OCC2CCCO2)nc2c1[nH]c(=O)n2CC1CCOCC1
Reaction #192788
DOI: 10.1039/C8SC04228D
CC1COC2C(Br)COC12
Reaction #204166
DOI: 10.1039/C8SC04228D
COCCOc1cc2c(Cl)nc(Nc3cc(C)[nH]n3)cc2cc1OC1CCOC1
Reaction #210001
DOI: 10.1039/C8SC04228D
Cc1sc(-c2cccc(-c3ccccc3)c2)nc1CCOc1ccc(OC(C)(C)C(=O)O)cc1
Reaction #211505
DOI: 10.1039/C8SC04228D
1 ページ次のページ