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13785

OCc1cnc(CO)n1Cc1ccccc1
Reaction #9003
2,5-bis-(hydroxymethyl)-N-benzylimidazole
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-]
Reaction #9004
monoacetate
DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81268
title compound
Ausbeute 76.5%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81269
title compound
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81270
title compound
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81271
title compound
Ausbeute 52.5%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)OCOC(=O)C(C)(C)C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81272
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81273
title compound
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81274
title compound
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81275
title compound
Ausbeute 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)[O-])n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Li+]
Reaction #81276
lithium 2-ethoxymethyl-4-(1-hydroxyl-methylethyl)-1-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81277
title compound
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OCc1nc(C(C)(C)O)c(C(=O)OC(C)C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81278
title compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OCc1nc(C(C)(C)O)c(C(=O)OC(C)C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81279
title compound
Ausbeute 95.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81280
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(C)(C)O)nc(C(C)OC)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81281
title compound
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)OC)n1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #81282
title compound
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #81283
title compound
Ausbeute 98.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1
Reaction #81284
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCOCc1nc(C(C)(C)O)c(C(=O)OCCC)n1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #81285
title compound
Ausbeute 75.6%DOI: 10.6084/m9.figshare.5104873.v1
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