Поиск подструктуры

6489

CC(C)=CCOCC1CO1
Reaction #75447
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(OC[C@@H]1CO1)C(F)(F)F
Reaction #95561
(S)-3-trifloxy-1,2-epoxypropane
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
C1CC[C@]23O[C@H]2CCOC3C1
Reaction #160802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C1CC2O[C@@]23COCC[C@@H]3C1
Reaction #160813
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@]12COCC[C@@H]1CCC[C@H]2Nc1ccc(F)cc1
Reaction #160814
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1COC[C@H]1NCc1ccccc1
Reaction #168346
trans-4-(benzylamino) tetrahydrofuran-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(c2ccc(Cl)cc2)CO1
Reaction #169553
methyl 2-(4-chlorophenyl)oxirane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(O)CCl)cc2oc3ccccc3c(=O)c12
Reaction #170283
title compound
Выход 71.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(C3CCCCC3)c(-c3ccccc3OCC3CO3)[nH]c2c1
Reaction #174474
DOI: 10.1039/C8SC04228D
COC(=O)C(C)(C)NC(=O)c1ccccc1OCC(O)CN1CCC(Oc2ccc(F)c(F)c2)CC1
Reaction #174631
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(CCCCOc2ccccc2)CO1
Reaction #176701
DOI: 10.1039/C8SC04228D
CC(C)=CCOCC1CO1
Reaction #185939
DOI: 10.1039/C8SC04228D
Cc1cc(OCC2CO2)ccc1C=O
Reaction #186905
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(CCCC2CCCCC2)CO1
Reaction #189951
DOI: 10.1039/C8SC04228D
COc1cc2c(Oc3cc(C)c(C)nc3-c3ccc(C)cn3)ccnc2cc1OCC1CO1
Reaction #207185
DOI: 10.1039/C8SC04228D
COC(=O)CCC(=O)c1ccc(C)cc1OCC(O)CNC(C)(C)C
Reaction #209279
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)c1c(-c2ccc(OCC3CO3)cc2)oc2ccccc12
Reaction #209608
DOI: 10.1039/C8SC04228D
OC1COCC1OCc1ccccc1
Reaction #209967
DOI: 10.1039/C8SC04228D
O=C(Cc1ccccc1)c1ccc(OCC2CO2)cc1
Reaction #217092
4-Glycidyloxyphenyl benzyl ketone
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(C)oc2cc(Oc3ccnc4cc(OCC5CO5)ccc34)ccc12
Reaction #217858
N,2-dimethyl-6-{[7-(oxiran-2-ylmethoxy)quinolin-4-yl]oxy}-1-benzofuran-3-carboxamide
Выход 93.8%DOI: 10.6084/m9.figshare.5104873.v1
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