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4500

CCOC(=O)CC(=O)COCC1OC(C)(C)OC1COCC(=O)CC(=O)OCC
Reaction #1344
title compound
Ausbeute 43.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)COCC1COC(C)(C)O1
Reaction #1345
title compound
Ausbeute 50.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(CCl)N2CCOC2(C)C(C(=O)OC)C1c1ccccc1Cl
Reaction #1350
title compound
Ausbeute 17.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1coc(-c2ccccc2)n1
Reaction #4495
ethyl 2-phenyl-4-oxazoleacetate
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1csc(C2CCCCC2)n1
Reaction #4496
ethyl 2-cyclohexyl-4-thiazoleacetate
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(CCl)c2ccc(O)cc2o1
Reaction #43923
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCON=C(C(=O)CCl)C(=O)OCC
Reaction #55544
ethyl 4-chloro-3-oxo-2-propargyloxyiminobutyrate
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1
C#CCON=C(C(=O)OCC)c1csc(N)n1
Reaction #55545
ethyl 2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetate
Ausbeute 53.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=NOCCOC(=O)c1ccccc1)C(=O)CCl
Reaction #55548
ethyl 2-(2-benzoyloxyethoxyimino)-4-chloro-3-oxobutyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=NOCCOC(=O)c1ccccc1)c1csc(N)n1
Reaction #55549
ethyl 2-(2-aminothiazol-4-yl)-2-(2-benzoyloxyethoxyimino)acetate
Ausbeute 29.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1csc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)n1
Reaction #71792
title compound
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(O)CCl
Reaction #77181
4-chloro-3-hydroxybutyric acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1csc(-c2ccccc2O)n1
Reaction #81854
4a
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(CCl)c2cc(F)c(O)c(F)c2o1
Reaction #91172
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cn2c(=O)cc(CCl)nc2s1
Reaction #92916
7-chloromethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(CCl)nc(C(Cl)(Cl)Cl)n1
Reaction #95000
crude product
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)CSC(C)(C)C
Reaction #164679
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1coc(C2CC2)n1
Reaction #169391
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)COCCn1c(C)ccc1C
Reaction #180634
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(N)CCl
Reaction #185978
DOI: 10.1039/C8SC04228D
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