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1864

CCN(CCCOC)C(=N)N
Reaction #859
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCNC(=N)N
Reaction #860
title compound
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCOCCOC(=O)c1ccccc1
Reaction #861
title compound
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOCCNC(=N)N
Reaction #862
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CON=Cc1[nH]ccc1S(=O)(=O)NC(C)(C)C
Reaction #917
title compound
Ausbeute 96.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=NO)C(=NO)C[C@]4(C)[C@H]3CC[C@]12C
Reaction #928
17β-Acetoxy-2,3-dihydroxyimino-5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]c2c1C(=O)CCC2
Reaction #997
ethyl 4-oxo-4,5,6,7-tetrahydroindole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]c2c1C(=O)CCCC2
Reaction #1001
ethyl 4-oxo-1,4,5,6,7,8-hexahydro-cyclohepta[b]pyrrole-3-carboxylate
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]c2c1C(=O)N(CC)CC2
Reaction #1003
ethyl 4-oxo-5-ethyl-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine-3-carboxylate
Ausbeute 53.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)COc1ccc(C#N)cc1
Reaction #1019
desired product
Ausbeute 27.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)ccc1OCC(C)N
Reaction #1020
desired product
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #1021
desired product
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=NO)c1nccc2ccccc12
Reaction #1026
1-acetyl-isoquinoline oxime
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=NO)c1cc2ccccc2cn1
Reaction #1028
3-acetyl-isoquinoline oxime
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=NO)c1nccc(-c2ccccn2)n1
Reaction #1029
2-acetyl-4-(pyrid-2-yl)-pyrimidine oxime
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #1262
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Ausbeute 41.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C=C/c2cccc3c2C(Sc2ccccc2)=CCC3(C)C)cc1
Reaction #1466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C=C/c2ccc3c(c2)C(SCC)=CCC3(C)C)cc1
Reaction #1467
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(=O)[nH]c(-c2ccccc2)n1
Reaction #1540
6-ethoxy-2-phenyl-4(3H)-pyrimidinone
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
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