Участвует в 12 реакциях

Fc1ccc(C2OCCO2)cn1

Fc1ccc(C2OCCO2)cn1
Reaction #648193
title compound
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Fc1ncc(C2OCCO2)cc1I
Reaction #648194
title compound
Выход 60.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Fc1ccc(C2OCCO2)cn1
Reaction #1311734
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Fc1ccc(C2OCCO2)cn1
Reaction #1708590
5-(1,3-dioxolan-2-yl)-2-fluoropyridine
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
OB(O)c1cc(C2OCCO2)cnc1F
Reaction #1708591
5-(1,3-dioxolan-2-yl)-2-fluoropyridin-3-ylboronic acid
Выход 67.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Fc1ccc(C2OCCO2)cn1
Reaction #1708913
5-(1,3-dioxolan-2-yl)-2-fluoropyridine
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
OB(O)c1cc(C2OCCO2)cnc1F
Reaction #1708914
product
Выход 61.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Fc1ccc(C2OCCO2)cn1
Reaction #1899002
5-(1,3-dioxolan-2-yl)-2-fluoropyridine
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
OB(O)c1cc(C2OCCO2)cnc1F
Reaction #1899003
5-(1,3-dioxolan-2-yl)-2-fluoropyridin-3-ylboronic acid
Выход 67.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
Fc1ccc(C2OCCO2)cn1
Reaction #1899321
5-(1,3-dioxolan-2-yl)-2-fluoropyridine
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
OB(O)c1cc(C2OCCO2)cnc1F
Reaction #1899322
product
Выход 61.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
Fc1ccc(C2OCCO2)cn1
Reaction #2223765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)