#903708

Cn1nccc1B(O)O
Reaction #74615
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cn1nccc1B(O)O
Reaction #159877
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1nccc1B1OC(C)(C)C(C)(C)O1
Reaction #176735
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1nccc1B1OC(C)(C)C(C)(C)O1
Reaction #195850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C)c(OCc2ccccc2C(=O)c2ccnn2C)c1
Reaction #232416
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1cccn1
Reaction #247059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccnn1C
Reaction #264695
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(C(O)c2ccnn2C)c(Cl)c(Cl)c1OC
Reaction #270811
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(C)c(OCc2ccccc2C(=O)c2ccnn2C)c1
Reaction #299117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccnn1C
Reaction #303545
1-methyl-5-(tributylstannyl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cn1nccc1B1OC(C)(C)C(C)(C)O1
Reaction #341915
1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1ccc(C)c(OCc2ccccc2C(=O)c2ccnn2C)c1
Reaction #366631
2-(2,5-dimethylphenoxymethyl)phenyl 1-methylpyrazol-5-yl ketone
Ausbeute 15.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cn1nccc1[C@H]1CCCC[C@@H]1O
Reaction #424891
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1[C@H]1CCC[C@@H]1O
Reaction #424899
title compound
Ausbeute 21.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1[C@H]1CCCCC[C@@H]1O
Reaction #424901
title compound
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1[C@H]1C[C@H](OCc2ccccc2)CC[C@@H]1O
Reaction #425090
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1C1(O)CCCCC1
Reaction #425111
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1[C@H]1CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1O
Reaction #425182
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1[C@H]1C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@@H]1O
Reaction #425184
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1cc(S(=O)(=O)Cl)cn1
Reaction #640680
1-Methyl-1H-pyrazole-4-sulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
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