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271483

CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81233
title compound
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81234
title compound
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81263
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #262505
DOI: 10.1039/C8SC04228D
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #288335
DOI: 10.1039/C8SC04228D
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #352277
title compound
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #352304
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #384401
DOI: 10.1039/C8SC04228D
OC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #641195
Triphenyl carbinol
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #641199
Trityl Olmesartan Medoxomil
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #641201
trityl Olmesartan
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #746135
title compound
Ausbeute 71.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #2134447
olmesartan medoxomil
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1