2-methylbenzoxazole

Cc1nc2ccc(S(=O)(=O)Cl)cc2o1
Reaction #171959
Compound 8
Ausbeute 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
BrCc1nc2ccccc2o1
Reaction #196782
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc2ccc(S(=O)(=O)Cl)cc2o1
Reaction #496882
Compound 8
Ausbeute 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
BrCc1nc2ccccc2o1
Reaction #689968
2-bromomethyl-benzooxazole
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CN(C)/C=C/c1nc2ccccc2o1
Reaction #956099
title compound
Ausbeute 51.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
[I-]
Reaction #1039841
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
[I-]
Reaction #1042131
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC[n+]1c(C)oc2ccccc21.[I-]
Reaction #1119809
ethyl-2-methyl-benzoxazolium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_09
Cc1nc2ccc(S(=O)(=O)Cl)cc2o1
Reaction #1288978
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCCCC[n+]1c(C)oc2ccccc21.[I-]
Reaction #1464563
3-n-pentyl-2-methylbenzoxazolium iodide
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
CCCCCCCC[n+]1c(C)oc2ccccc21.[I-]
Reaction #1464564
3-n-octyl-2-methylbenzoxazolium iodide
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
Cc1nc2cccc(B3OC(C)(C)C(C)(C)O3)c2o1
Reaction #1577609
Ausbeute 43.0%DOI: 10.1021/ja412563eBorylation dataset from Roche
Cc1nc2cccc(B3OC(C)(C)C(C)(C)O3)c2o1
Reaction #1577610
Ausbeute 68.0%DOI: 10.1021/ja412563eBorylation dataset from Roche
Cc1nc2cccc(B3OC(C)(C)C(C)(C)O3)c2o1
Reaction #1577611
Ausbeute 51.0%DOI: 10.1021/ja412563eBorylation dataset from Roche
CCCCC[n+]1c(C)oc2ccccc21
Reaction #1649479
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
BrCc1nc2ccccc2o1
Reaction #1684997
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_04
Cc1nc2ccc(S(=O)(=O)Cl)cc2o1
Reaction #1778823
Compound 8
Ausbeute 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
c1ccc2ocnc2c1
Reaction #1810713
benzoxazole
Ausbeute 196.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_08
Cc1nc2ccc(S(=O)(=O)Cl)cc2o1
Reaction #2030116
Compound 8
Ausbeute 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
Cc1nc2cccc(B3OC(C)(C)C(C)(C)O3)c2o1
Reaction #2117124
DOI: 10.1038/s4155739k HTE dataset from Pfizer
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