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400675

CCCCCCCCCCCC1CC[C@@H](O)C(=O)O1
Reaction #6153
tetrahydro-3-hydroxy-(R)-6-undecyl-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCOc1ccc(C(=O)OC2(C(=O)OCC(C)CC)C=CC(c3ccccc3)=CC2)cc1
Reaction #6412
ester
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCOc1ccc(C(=O)OC2(C(=O)OCC(C)CC)C=CC(c3ccccc3)=CC2)cc1
Reaction #6418
ester
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C1OC(OCC)C=CC1C
Reaction #56362
butyl-3-methyl-6-ethoxy-3,6-dihydro-2H-pyran-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(=O)OC(C)C(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93010
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C(C)(C)Oc1ccc2c(c1)c(-c1ccc(Cl)cc1)c(C)n2C
Reaction #95171
2-[3-(4-Chloro-phenyl)-1,2-dimethyl-1H-indole-5-yloxy]-2-methyl-propanoic acid butylester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOC(=O)C(C)(C)Oc1ccc2c(c1)c(-c1ccc(Cl)cc1)c(C)n2C
Reaction #95172
2-[3-(4-Chloro-phenyl)-1,2-dimethyl-1H-indole-5-yloxy]-2-methyl-propanoic acid amylester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCCCC1Cl)C1CC(c2csc(C3CCN(C(=O)Cn4nc(C(F)F)cc4C(F)F)CC3)n2)=NO1
Reaction #157984
2-Chlorocyclohexyl 3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@](O)(CCCC(C)(C)O)C(=O)O[C@@H]1C(OC)=C[C@]23CCCN2CCc2cc4c(cc2[C@H]13)OCO4
Reaction #159241
epi-homoharringtonine
Ausbeute 0.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCOC(=O)[C@](C)(O)CN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)NC(=O)c1cc(O)no1
Reaction #171387
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C1(C)COC(c2cc([N+](=O)[O-])ccc2Cl)O1
Reaction #187352
DOI: 10.1039/C8SC04228D
CCCCOC(=O)C(C)Oc1cccc(Oc2ccc(CN(Cc3ccccc3)c3cccc([N+](=O)[O-])c3C)cc2)c1
Reaction #190534
DOI: 10.1039/C8SC04228D
O=C([O-])C(F)(F)F
Reaction #203209
DOI: 10.1039/C8SC04228D
O=C(O)C(O)c1ccccc1
Reaction #215673
mandelic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](O)c1ccccc1
Reaction #215674
D-(-)-mandelic acid
Ausbeute 72.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](O)c1ccccc1
Reaction #215675
D-(-)-mandelic acid
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCO[C@@H](CC(C)C)C(=O)O
Reaction #220194
compound 10
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(C)c(OC)c(CC2OC2(C)CO)c1C
Reaction #225398
DOI: 10.1039/C8SC04228D
CC1(C)CCCC2(C)C1CCC1(C)OC(O)C(O)C12
Reaction #227460
DOI: 10.1039/C8SC04228D
CCCCOC(=O)C(CC)Oc1cccc(C=O)c1
Reaction #227698
DOI: 10.1039/C8SC04228D
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