Teilstruktursuche

323773

OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66028
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66029
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66030
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CCC)C(=O)OCCCCO
Reaction #70095
oil
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCCC1(O)CCCC1)C1CC2CC1C1C3C=CC(C3)C21
Reaction #268294
DOI: 10.1039/C8SC04228D
C=C1C[C@@]23CC[C@H]4[C@@](C)(CCC[C@@]4(C)C(=O)O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H]2CC[C@]1(O[C@@H]1O[C@H](C)[C@@H](O)[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O)C3
Reaction #310524
rebaudioside C
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #310525
sulfopropyl ester
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #475364
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #475365
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@H](C)CC[C@]2(C(=O)O[C@@H]3O[C@H](CO[C@@H]4O[C@H](CO)[C@@H](O[C@@H]5O[C@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@@H](O)[C@H](O)[C@H]3O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)[C@@](C)(CO)[C@@H]5CC[C@]43C)[C@H]12
Reaction #536954
asiaticoside
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NS(=O)(=O)c2ccccc21
Reaction #567707
Saccharine
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #598944
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #598945
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #792147
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #792148
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@H](C)CC[C@]2(C(=O)O[C@@H]3O[C@H](CO[C@@H]4O[C@H](CO)[C@@H](O[C@@H]5O[C@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@@H](O)[C@H](O)[C@H]3O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)[C@@](C)(CO)[C@@H]5CC[C@]43C)[C@H]12
Reaction #836581
asiaticoside
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CCC)C(=O)OCCC(COC(=O)C(CCC)CCC)OC(=O)C(CCC)CCC
Reaction #992446
1,2,4-butanetriol tri-(di-n-propylacetate)
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #995255
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #995256
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1C2CC3C(OC(=O)C31)C2OC(=O)C12CC3CC(CC(C3)C1)C2
Reaction #1013620
target compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
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