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CC1=C[C@H]2[C@@]3(O)[C@H](C)[C@@H](O)[C@]4(O)[C@H]([C@@H]3C=C(CO)C[C@]2(O)C1=O)C4(C)C
Reaction #71613
phorbol
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74825
compound ( 2-b )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74826
compound ( 2-b )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC)C(O)CCC1CC(=O)OC
Reaction #74829
compound ( 1-b )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(O)CCC1CC(=O)OC
Reaction #74830
compound ( 1-b )
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CC=CC1=O
Reaction #89689
5-allylcyclopent-2-enone
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CC(NC(=O)OC(C)(C)C)CC1=O
Reaction #89690
tert-butyl 3-allyl-4-oxocyclopentylcarbamate
Ausbeute 27.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CC(NC(=O)OCc2ccccc2)CC1=O
Reaction #89691
benzyl 3-allyl-4-oxocyclopentylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CC(C[N+](=O)[O-])CC1=O
Reaction #89693
compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1=C(C)C(O)CC1=O
Reaction #96294
2-allyl-3-methyl-4-hydroxy-2-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1=C(C)C(O)CC1=O
Reaction #96296
2-allyl-3-methyl-4-hydroxy-2cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1=C(C)C(O)CC1=O
Reaction #96297
2-allyl-3-methyl-4-hydroxy-2-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC(=O)[C@@]1(O)C(O)=C(C(=O)CC(C)C)C(=O)[C@@H]1CCC(C)C
Reaction #160560
(+)-KDT-500
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)O)C[C@H](C)C[C@H](C)C(=O)/C=C(\O)[C@H](C)C[C@H](C)C/C=C/[C@@H](C)[C@@H](O)[C@@H](C)[C@@H](O)C[C@@H]1CC[C@@](C)([C@H]2CC[C@@](C)([C@@H](C)O)O2)O1
Reaction #218731
ionomycin
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)O)C[C@H](C)C[C@H](C)C(=O)/C=C(\O)[C@H](C)C[C@H](C)C/C=C/[C@@H](C)[C@@H](O)[C@@H](C)[C@@H](O)C[C@@H]1CC[C@@](C)([C@H]2CC[C@@](C)([C@@H](C)O)O2)O1
Reaction #218820
Ionomycin
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C(=O)C=CC1=O
Reaction #297958
DOI: 10.1039/C8SC04228D
C=CCC1C(=O)C=CC1(C)O
Reaction #310965
2-allyl-3-hydroxy-3-methyl-4-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C(=O)C=CC1(C)O
Reaction #310968
2-allyl-3-hydroxy-3-methyl-4-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C(=O)C=CC1(C)O
Reaction #310969
2-allyl-3-hydroxy-3-methyl-4-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@H]1C(=O)C=C[C@@H]1/C=C/[C@@H](O)CCc1cc(Br)c(C)s1
Reaction #337962
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Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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