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C=CCN(CC=C)C(=O)CCl
Reaction #3721
2-chloro-N,N-diallylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)N=C(c2cc(Cl)cc(Cl)c2)OC1(Cl)C(Cl)Cl
Reaction #429933
2-(3',5'-dichlorophenyl)-4,4-dimethyl-5-chloro-5-dichloromethyloxazoline
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(CC=C)C(=O)CCl
Reaction #575524
2-Chloro-N,N-diallylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)N=C(c2cc(Cl)cc(Cl)c2)OC1(Cl)C(Cl)Cl
Reaction #708112
2-(3',5'-dichlorophenyl)-4,4-dimethyl-5-chloro-5-dichloromethyloxazoline
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(CC=C)C(=O)CCl
Reaction #1696062
2-Chloro-N,N-diallylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
Br.CC1(C)N=C(c2cc(Cl)cc(Cl)c2)OC1=CBr
Reaction #1867185
2-(3',5'-dichlorophenyl)-4,4-dimethyl-5-bromomethylenoxazoline hydrobromide
Rendimiento 178.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)N=C(c2cc(Cl)cc(Cl)c2)OC1(Cl)C(Cl)Cl
Reaction #1867190
2-(3',5'-dichlorophenyl)-4,4-dimethyl-5-chloro-5-dichloromethyloxazoline
DOI: 10.6084/m9.figshare.5104873.v1