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383975

O[C@@H]1C=Cc2ccccc21
Reaction #3105
(R)-inden-1-ol
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1C=Cc2ccccc21
Reaction #3106
(R)-1-acetoxyindene
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(=O)C[C@@H](CC#N)O[Si](C)(C)C(C)(C)C
Reaction #5779
(R)-1,1-dimethylethyl 6-cyano-5-[(1,1-dimethylethyl)dimethylsilyl]oxy-3-oxohexanoate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CC)OC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6397
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2ccc3c(c2)nc(Nc2cccc(-c4cn(Cc5ccccc5)nn4)c2)n3C)ccn1
Reaction #41788
4-{2-(3-(1-Benzyl-1H-[1,2,3]triazol-4-yl)-phenyl amino]-1-methyl-1H-benzoimidazol-5-yloxy}-pyridine-2-carboxylic acid methyl amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cn(Cc2ccccc2)nn1)C(=O)OCc1ccccc1
Reaction #46653
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccccc1C1(OCCCOC2(c3ccccc3C#C)C=CN3C(=O)c4cc(OC)ccc4N=C[C@H]32)C=CN2C(=O)c3cc(OC)ccc3N=C[C@H]21
Reaction #47143
glass
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cn(Cc2ccccc2)nn1)C(=O)OCc1ccccc1
Reaction #49143
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC(C)(C)C
Reaction #49695
tert-butyl propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC(C)(C)C
Reaction #49696
tert-butyl propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC(C)(C)C
Reaction #49697
tert-butyl propanoate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc2c(c(=O)[nH]1)NC(CNc1ccc(C(=O)N[C@@H](CCC(=O)O)C(=O)O)cc1)CN2
Reaction #54546
tetrahydrofolic acid
Ausbeute 0.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCCN1c2ccccc2CCc2ccccc21
Reaction #57129
desipramine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23.C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23.O
Reaction #59650
levofloxacin hemihydrate
Ausbeute 554.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(O)cc(-c3ccccc3)nc2c1
Reaction #61357
4-hydroxy-2-phenyl-7-methoxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2.O=C1O[C@H]([C@@H](O)CO)C([O-])=C1O
Reaction #62722
title compound
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)CC[C@@H]1[C@H]2Cc3cccc(OCC(=O)O)c3C[C@H]2C[C@H]1O
Reaction #67896
titled compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@H]2[C@@H]3CCC(=O)[C@@]3(C)CC[C@@H]2[C@@]2(C)CCC(=O)C[C@]12O
Reaction #70381
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCn3cc(CO)nn3)cc2)c(F)c1)C(=O)N=C(N)N
Reaction #73973
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75332
Hydrated hafnium-ammonium-ascorbate
DOI: 10.6084/m9.figshare.5104873.v1
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