2-(4-chlorophenoxy-methyl)-2-tert.-butyl-oxirane

CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #4220
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1yl)butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #4221
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #417621
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #417622
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #458666
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_07
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #458667
2-(4-chlorophenoxy-methyl)-2-tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_07
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #501225
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #501226
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Выход 83.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #564382
2-(4-chlorophenoxymethyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanol
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_12
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #1066632
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #1175139
2-(4-chlorophenoxymethyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanol
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #1252865
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_03
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #1252866
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_03
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #1252886
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_03
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #1252887
2-(4-chlorophenoxy-methyl)-2tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_03
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #1287058
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazole-1-yl)butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_02
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #1287059
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_02
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #1336047
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_12
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #1336048
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_12
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #1349656
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_06
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