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2561

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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 32.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(-c3ncon3)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48833
title compound
Выход 84.5%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(-c3ncon3)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48834
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67194
N-{[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}BUTAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
CCN(Cc1ccccc1)C[C@H]1COc2ccc(SC)c(F)c2O1
Reaction #67300
title compound
Выход 51.3%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
CCCCNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #187462
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
Cc1ccc(S(=O)(=O)OC(C)COc2c(N)ccc(F)c2F)cc1
Reaction #198105
DOI: 10.1039/C8SC04228D
CC1COC2C(Br)COC12
Reaction #204166
DOI: 10.1039/C8SC04228D
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