(S)-Glycidyl-3-nitrobenzenesulphonate

Oc1cccc(C[C@H]2CO2)c1OCc1ccccc1
Reaction #1614
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1cccc(OCc2ccccc2)c1C[C@H]1CO1
Reaction #1615
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc(OCc2ccccc2)cc1C[C@H]1CO1
Reaction #1616
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1c(OC[C@@H]2CO2)cccc1[N+](=O)[O-]
Reaction #53515
title product
المردود 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(OC[C@@H]2CO2)cn1
Reaction #68908
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc2c(c1)[nH]c1cccc(OC[C@@H]3CO3)c12
Reaction #68909
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)Nc1ccccc1OC[C@@H]1CO1
Reaction #357236
subtitled compound
المردود 64.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(=O)Nc1ccc(F)cc1OC[C@@H]1CO1
Reaction #357238
subtitled compound
المردود 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1ccc(NC(C)=O)c(OC[C@@H]2CO2)c1
Reaction #357240
crude product
المردود 122.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C(NC1CC1)c1ccccc1OC[C@@H]1CO1
Reaction #357244
subtitled compound
المردود 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C(NC1CC1)c1ccc(F)cc1OCC1CO1
Reaction #357246
subtitled compound
المردود 59.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1ccc(C(=O)NC2CC2)c(OC[C@@H]2CO2)c1
Reaction #357248
subtitled compound
المردود 112.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(=O)Nc1cc(Cl)ccc1OC[C@@H]1CO1
Reaction #357254
subtitled compound
المردود 92.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(=O)Nc1ccc(Cl)cc1OC[C@@H]1CO1
Reaction #357256
subtitled compound
المردود 73.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(=O)Nc1cc(C(F)(F)F)ccc1OC[C@@H]1CO1
Reaction #357259
subtitled compound
المردود 42.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C(NC1CC1)c1ccc(OC(c2ccccc2)(c2ccccc2)c2ccccc2)cc1OC[C@@H]1CO1
Reaction #357262
subtitled compound
المردود 70.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(=O)Nc1ccc(OC(C)=O)cc1OC[C@@H]1CO1
Reaction #357270
titled compound
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CNC(=O)c1ccccc1OC[C@@H]1CO1
Reaction #357284
subtitled compound
المردود 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COC(=O)c1ccc(F)cc1OC[C@@H]1CO1
Reaction #357287
subtitled compound
المردود 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COC(=O)c1ccc(C)cc1OC[C@@H]1CO1
Reaction #357288
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
الصفحة 1التالي