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19469

O=C(O)c1coc2c1C(=O)CCC2
Reaction #995
4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #1177
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)CC(=O)c1c(C)cc(C)cc1C
Reaction #1248
red oil
Ausbeute 66.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1csc(N)n1
Reaction #2724
Ethyl 2-amino-thiazol-4-yl-glyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)[O-].[K+]
Reaction #4059
Potassium ethyl oxalate
Ausbeute 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(Cc1cc(OC)ccc1Br)C(=O)OCC
Reaction #5440
desired product
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CCc1cc(OC)ccc1Br)C(=O)OCC
Reaction #5449
desired product
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2c(Cl)cccc2n1
Reaction #5524
desired product
Ausbeute 67.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6499
2-ethoxalyloxyethyl methacrylate
Ausbeute 76.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6500
2-ethoxalyloxyethyl methacrylate
Ausbeute 76.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6501
2-ethoxalyloxyethyl methacrylate
Ausbeute 56.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6502
2-ethoxalyloxyethyl methacrylate
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(CCOC(=O)C(=O)OCC)cc1
Reaction #6503
aimed compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1ccc2ccccc21
Reaction #6798
N-ethyl-indole
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CC)NC(C)=O
Reaction #7632
Ethyl 3-(acetylamino)-2-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CC)NC(=O)C1CCCC1
Reaction #7645
Ethyl 3-[(cyclopentylcarbonyl)amino]-2-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(OCc3cccc(F)c3)ccc2c(=O)n1CC(N)=O
Reaction #7726
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)(CC(=O)c1ccc(C)c(F)c1)C(=O)OCC
Reaction #8005
title compound
Ausbeute 79.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8529
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8531
title compound
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1
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