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OCC(O)CO

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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCC(C)(C)N1[O].NCCNC(=O)Cc1cccc(NC(=O)Cc2ccc(Nc3ncnc4c3ncn4[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)cc2)c1
Reaction #6519
TEMPO ADAC
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1[C@H](O)[C@@H](COC2CC2)O[C@H]1n1cnc2c(NCc3cccc(I)c3)nc(Cl)nc21
Reaction #6770
N6-(3-Iodobenzyl)-2-chloro-5′-O-cyclopropyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@@]2(COS(=O)(=O)c3ccc(C)cc3)O[C@@H](n3cc(C)c(=O)[nH]c3=O)[C@H](O)[C@H]2OCc2ccccc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #6875
nucleoside
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cc(F)c2c(c1)OC(CO)CO2
Reaction #67280
title compound
Ausbeute 33.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2COc3c(F)cc(S(C)(=O)=O)cc3O2)cc1
Reaction #67281
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cc(F)c2c(c1)O[C@@H](CO)CO2
Reaction #67285
[(2S)-5-FLUORO-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHANOL
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC[C@H]2COc3c(F)cc(S(C)(=O)=O)cc3O2)cc1
Reaction #67286
[(2R)-5-FLUORO-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL 4-METHYLBENZENESULFONATE
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOC[C@H](O)CO)ccc3cnsc23)c(F)c1
Reaction #166257
title compound
Ausbeute 26.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC1OC(c2ccc(Cl)c(Cc3ccc(-c4ccc(C=O)c(F)c4)s3)c2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #173799
DOI: 10.1039/C8SC04228D
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