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COC(=O)/C(C)=C\C[C@@]12OC(C)(C)[C@@H]3C[C@@H](C=C4C(=O)c5c(O)c6c(c(CC=C(C)C)c5O[C@]431)O[C@](C)(CCC=C(C)C)C=C6)C2=O
Reaction #821361
methyl gambogate
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC[C@]1(C)C=Cc2c(O)c3c(c(CC=C(C)C)c2O1)O[C@]12C(=C[C@@H]4C[C@H]1C(C)(C)O[C@@]2(C/C=C(/C)C(=O)O)C4=O)C3=O
Reaction #821837
gambogic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC[C@]1(C)C=Cc2c(O)c3c(c(CC=C(C)C)c2O1)O[C@]12C(=C[C@@H]4CC1C(C)(C)OC2(C/C=C(\C)C(=O)O)C4=O)C3=O
Reaction #821838
Isogambogic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(C)=C\C[C@@]12OC(C)(C)[C@@H]3C[C@@H](C=C4C(=O)c5c(O)c6c(c(CC=C(C)C)c5O[C@]431)O[C@](C)(CCC=C(C)C)C=C6)C2=O
Reaction #1077881
title compound
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC[C@]1(C)C=Cc2c(O)c3c(c(CC=C(C)C)c2O1)O[C@]12C(C[C@@H]4C[C@H]1C(C)(C)O[C@@]2(C/C=C(/C)C(=O)O)C4=O)C3=O
Reaction #1077882
title compound
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O[Si](C(C)C)(C(C)C)C(C)C)cc2occ(N3CCC(O)(c4ccc(F)cc4)CC3)c(=O)c2c1Br
Reaction #1090794
5-bromo-6-methyl-7-triisopropylsilyloxy-3-(4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl)-chromen-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(c(C)c1O[Si](C(C)C)(C(C)C)C(C)C)OCCC2=O
Reaction #1090805
6,8-Dimethyl-7-triisopropylsilyioxychroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1O[Si](C(C)C)(C(C)C)C(C)C)OCCC2=O
Reaction #1090807
6-methyl-7-triisopropylsilyloxychroman-4-one
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(C)=C\C[C@@]12OC(C)(C)[C@@H]3C[C@@H](C=C4C(=O)c5c(O)c6c(c(CC=C(C)C)c5O[C@]431)O[C@](C)(CCC=C(C)C)C=C6)C2=O
Reaction #1253242
title compound
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O[Si](C(C)C)(C(C)C)C(C)C)cc2occ(N3CCC(O)(c4ccc(F)cc4)CC3)c(=O)c2c1Br
Reaction #1471490
5-bromo-6-methyl-7-triisopropylsilyloxy-3-(4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl)-chromen-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(c(C)c1O[Si](C(C)C)(C(C)C)C(C)C)OCCC2=O
Reaction #1471502
6,8-Dimethyl-7-triisopropylsilyloxychroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1O[Si](C(C)C)(C(C)C)C(C)C)OCCC2=O
Reaction #1471504
6-methyl-7-triisopropylsilyloxychroman-4-one
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C=O)c(O)cc2c1C(=O)CC(C)(C)O2
Reaction #1603865
7-Hydroxy-5-methoxy-2,2-dimethyl-4-oxochroman-6-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2ccc(O)c(-c3c(O)cc4oc(-c5ccc(O)cc5)cc(=O)c4c3O)c2)oc2cc(O)cc(O)c12
Reaction #2063529
robustaflavone
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2ccc(O)c(-c3c(O)cc4oc(-c5ccc(O)cc5)cc(=O)c4c3O)c2)oc2cc(O)cc(O)c12
Reaction #2063535
robustaflavone
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(c(C)c1O[Si](C(C)C)(C(C)C)C(C)C)OCCC2=O
Reaction #2429889
DOI: 10.1039/C8SC04228D
Cc1cc2c(cc1O[Si](C(C)C)(C(C)C)C(C)C)OCCC2=O
Reaction #2431748
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)Cc1ccc(OCC2(C)CC(=O)c3cc(C(C)=O)c(O)c(C)c3O2)cc1
Reaction #2438700
title compound
DOI: 10.6084/m9.figshare.5104873.v1