2-Fluoropyridine

O=Cc1cccnc1F
Reaction #7257
title compound
수율 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(Oc3ccccn3)CN2C1=O
Reaction #46099
14-tert-butoxycarbonylamino-2,15-dioxo-18-(pyridin-2-yloxy)-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
수율 57.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Brc1ccc(Oc2ccccn2)cc1
Reaction #68976
2-(4-bromo-phenoxy)pyridine
수율 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nc2ccccc2n1-c1ccccn1
Reaction #79182
titled compound
수율 71.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1cccc2c1nc(/C=C/c1ccccc1)n2-c1ccccn1.Cl
Reaction #79193
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=[N+]([O-])c1cc(C(F)(F)F)ccc1Nc1ccccn1
Reaction #79194
titled compound
수율 23.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1cc2nc(/C=C/c3ccccc3)n(-c3ccccn3)c2cc1C
Reaction #79211
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
OB(O)c1cccnc1F
Reaction #80410
2-fluoro-3-dihydroxyborylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(c1ccc(-c2cnco2)cc1)N(C1CC1)C1CCN(c2ccccn2)CC1
Reaction #156010
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1cccnc1F
Reaction #162386
2-fluoronicotinaldehyde
수율 45.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OCc1ccc(COc2ccccn2)cc1
Reaction #164981
title compound
수율 67.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc(OCc2ccc(C3OCCO3)cn2)nc1
Reaction #165339
title compound
수율 77.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1cc(COc2ccccn2)ccc1C1OCCO1
Reaction #165412
title compound
수율 64.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1ccc(Oc2ccccn2)cc1
Reaction #165431
title compound
수율 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Brc1ccc(COc2ccccn2)cc1
Reaction #165463
title compound
수율 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNCCN(C)c1ccccn1
Reaction #178687
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCc1cccnc1F
Reaction #183078
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cc(C(F)(F)F)ccc1Nc1ccccn1
Reaction #183179
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1cccnc1F
Reaction #193418
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)OC2CN=C(c3cccnc3F)C2(F)F)cc1
Reaction #196915
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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