EDOT

O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #75461
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(S(=O)(=O)O)cc1
Reaction #420670
p-toluenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scc2c1OCCO2
Reaction #454041
2-(tributylstannyl)-3,4-(ethylenedioxy)thiophene
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #500839
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scc2c1OCCO2
Reaction #517916
2-(tributylstannyl)-3,4-ethylenedioxythiophene
المردود 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scc2c1OCCO2
Reaction #517917
2-Tributylstannyl-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
Reaction #598916
quinones
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
Cc1ccc(S(=O)(=O)O)cc1
Reaction #603616
p-toluenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scc2c1OCCO2
Reaction #762757
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #927239
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scc2c1OCCO2
Reaction #1137869
tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane
المردود 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
O=Cc1scc2c1OCCO2
Reaction #1266701
3,4-Ethylenedioxythiophene-2-carboxaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #1446072
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
CC1(C)OB(c2scc3c2OCCO3)OC1(C)C
Reaction #1577824
المردود 85.0%DOI: 10.1021/jacs.7b08143Borylation dataset from Roche
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #1668644
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_05
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #1720621
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_01
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1s[c]([Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC)c2c1OCCO2
Reaction #1838501
oil 6
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #2021469
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_05
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #2172165
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_04
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #2206469
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_02
الصفحة 1التالي