sodium thiosulfate

O=CCCn1cnc2ccccc21
Reaction #7223
3-(benzimidazol-1-yl)propanal
Ausbeute 81.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cc(Br)oc1C
Reaction #9730
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(S(=O)(=O)CCC(=O)CC2CCCN2C(=O)OC(C)(C)C)cc1
Reaction #9982
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)S[C@@H](Cc1ccccc1)C(=O)O
Reaction #11024
(2S)-2-acetylthio-3-phenylpropionic acid
Ausbeute 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)S[C@@H](Cc1ccccc1)C(=O)O
Reaction #11026
(2S)-2-acetylthio-3-phenylpropionic acid
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #40585
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1cn(-c2ccc3c(c2)CCC3)c2nc(S(C)(=O)=O)ncc2c1=O
Reaction #40611
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc(Br)c2c(c1)CCO2
Reaction #43451
desired compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc(Br)c2c(c1)CCO2
Reaction #43639
desired compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(O)c(F)c(C)c1Br
Reaction #43920
title compound
Ausbeute 36.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)OC[C@H]1O[C@@H](n2cnc3c(Cl)nc(I)nc32)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #44331
[(2R,3R,4R,5R)-3,4-diacetyloxy-5-(6-chloro-2-iodopurin-9-yl)oxolan-2-yl]methyl acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOP(=O)(OCC)C1CC[C@H]2COC[C@@H](c3cc(F)c(F)c(F)c3)N2C1=O
Reaction #44629
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1C(I)CC[C@H]2CCC[C@@H](c3ccc(Cl)cc3)N12
Reaction #44645
(6S,9aR)-6-(4-chlorophenyl)-3-iodooctahydroquinolizin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(-c2coc3c(I)cnc(N)c23)ccc1NC(=O)OC(C)(C)C
Reaction #45469
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCC(CI)c1c(-c2ccccc2)c(C)c(C#N)c2nc(C3CC3)oc12
Reaction #45865
compound
Ausbeute 80.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(C2CCC(=O)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45869
compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[S@](=O)N[C@@H](Cc1cc(F)cc(Cl)c1)[C@@H](C=O)O[Si](C)(C)C(C)(C)C
Reaction #48284
solid/oil
Ausbeute 803.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCOC[C@H](NC(=O)OC(C)(C)C)[C@@H](C=O)O[Si](C)(C)C(C)(C)C
Reaction #48323
Tert-butyl (2S,3S)-1-(allyloxy)-3-(tert-butyldimethylsilyloxy)-4-oxobutan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](CO)Oc1cc(O)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48809
desired compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1ccc(Oc2cc(O[C@@H](C)CO)cc(C(=O)Nc3cc[nH]n3)c2)cc1
Reaction #48826
oil
Ausbeute 111.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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