Teilstruktursuche

1002460

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Reaction #93180
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=CC2=C(C(=O)c3c(O)c4c(c(O)c3C2=O)C(NCCO)CC(O)C4)C12OCCO2
Reaction #93181
7-(2-hydroxyethyl)amino-9-(1,1-ethylenedioxy)ethyl-6,9,11-trihydroxy-5,7,8,9,10,12-hexahydronaphthacene-5,12-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=CC2=C(C(=O)c3cc4c(c(O)c3C2=O)C(Br)CC(O)C4)C12OCCO2
Reaction #93182
7-bromo-9-(1,1-ethylenedioxy)ethyl-6,9-dihydroxy-5,7,8,9,10,12-hexahydronaphthacene-5,12-dione
Ausbeute 72.7%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #93183
crystals
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1(O)Cc2cc3c(c(O)c2C(NCCN(C)C)C1)C(=O)c1ccccc1C3=O
Reaction #93184
7-(2-dimethylaminoethyl)amino-9-acetyl-6,9-dihydroxy-5,7,8,9,10,12-hexahydronaphthacene-5,12-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC2(CC(C)(C)C1=O)OCC(C)O2
Reaction #94328
product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1(O)C(C)=CC(=O)CC1(C)C
Reaction #94329
4-Butyl-4-Hydroxy-3,5,5-Trimethyl-2-Cyclohexen-1-One
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1ccccc1C1C(C(=O)OCC)=C(C)NC(C=O)=C1C(=O)OCC
Reaction #193373
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(C)NC(C=O)=C(C(=O)OCC)C1c1ccccc1C(F)(F)F
Reaction #213581
DOI: 10.1039/C8SC04228D
COC(C=C(C)C=O)OC
Reaction #217161
4,4-dimethoxy-2-methyl-2-buten-1-al
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(C=O)NC(C)=C(C(=O)OCCN(CC)CC)C1c1cccc([N+](=O)[O-])c1
Reaction #227412
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(C)NC(C=O)=C(C(=O)OCC)C1c1cccc([N+](=O)[O-])c1
Reaction #229531
DOI: 10.1039/C8SC04228D
COC(=O)CCCCCCC1=C(C(OC)OC)CCC1=O
Reaction #246036
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(C=O)NC(C)=C(P2(=O)OCCCO2)C1c1ccccc1C(F)(F)F
Reaction #267887
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(C=O)NC(C)=C(C(=O)OCc2ccccc2)C1c1ccccc1[N+](=O)[O-]
Reaction #274429
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(C)NC(C=O)=C(C(=O)OC)C1c1ccccc1C#N
Reaction #276766
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(C=O)NC(C)=C(C(=O)OCCOCc2ccccc2)C1c1ccccc1[N+](=O)[O-]
Reaction #289447
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=CC2(CCC1S(=O)(=O)Nc1ccc(F)cc1Cl)OCC(NC(C)=O)CO2
Reaction #293229
DOI: 10.1039/C8SC04228D
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CO)O2
Reaction #311920
brown crystals
Ausbeute 111.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(C)=C/C(OC)OC
Reaction #329381
(E)-ethyl 4,4-dimethoxy-2-methylbut-2-enoate
Ausbeute 121.4%DOI: 10.6084/m9.figshare.5104873.v1
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