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CCOC(=O)C(N)=NO

CCOC(=O)c1nc(C(=O)OC(C)(C)C)c[nH]1
Reaction #1702
tert-butyl 2-ethoxycarbonylimidazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)=NOC(=O)c1cnccc1C(F)(F)F
Reaction #75494
Ethyl 2-Amino-2-(4-trifluoromethyl-3-pyridinecarbonyloxyimino)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(-c2cnccc2C(F)(F)F)n1
Reaction #75495
3-Ethoxycarbonyl-5-(4-trifluoromethyl-3-pyridyl)-1,2,4-oxadiazole
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)=NOC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #82813
ethyl 2-amino-2-(4-nitrobenzoyloxyimino)acetate
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)=NOC(=O)c1ccc(F)cc1
Reaction #82817
ethyl 2-amino-2-(4-fluorobenzoyloxyimino)acetate
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(N)=N/OC(=O)Cc1cc(F)ccc1F
Reaction #86851
(Z)-ethyl 2-amino-2-(2-(2,5-difluorophenyl)acetoxyimino)acetate
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2cc(F)ccc2F)n1
Reaction #86852
ethyl 5-(2,5-difluorobenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccsc2)n1
Reaction #86876
ethyl 5-(thiophen-3-ylmethyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 38.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccccc2C)n1
Reaction #86877
ethyl 5-(2-methylbenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccccc2Cl)n1
Reaction #86878
ethyl 5-(2-chlorobenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 38.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2cccc(Cl)c2)n1
Reaction #86879
ethyl 5-(3-chlorobenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccc(F)cc2F)n1
Reaction #86880
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2c(F)cccc2F)n1
Reaction #86881
ethyl 5-(2,6-difluorobenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2cccc(F)c2F)n1
Reaction #86882
ethyl 5-(2,3-difluorobenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccc(C(F)(F)F)cc2)n1
Reaction #86883
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2cccc(C(F)(F)F)c2)n1
Reaction #86884
ethyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccc(OC(F)(F)F)cc2)n1
Reaction #86885
ethyl 5-(4-(trifluoromethoxy)benzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 10.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2cccc(C)c2)n1
Reaction #86886
ethyl 5-(3-methylbenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 23.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccccc2OC)n1
Reaction #86887
ethyl 5-(2-methoxybenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 34.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccc(C)cc2)n1
Reaction #86888
ethyl 5-(4-methylbenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
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