Titanium

O=C(O)c1ccc2cc(C(=O)O)ccc2c1
Reaction #2476
2,6-naphthalenedicarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9836
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9837
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(C(=O)O)cc1
Reaction #47129
4-carboxybenzaldehyde
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1ccc(C(=O)O)cc1
Reaction #47130
4-carboxybenzaldehyde
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1ccc(C(=O)O)cc1
Reaction #47131
4-carboxybenzaldehyde
Ausbeute 70.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1ccc(C(=O)O)cc1
Reaction #47134
4-carboxybenzaldehyde
Ausbeute 63.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[Ti+4].[Ti+4].[Ti+4]
Reaction #157904
Titanium Borate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(O)c1ccccc1
Reaction #181621
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
—
Reaction #336643
mixture
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCCOC(=O)C(=O)c1ccc2c(c1)C1(C)CCN(C)C1N2C
Reaction #345332
1,2,3,3a,8,8a-hexahydro-α-oxo-1,3a,8 -trimethyl-5-pyrrolo[2,3-b]indole acetic acid, n-hexyl ester
Ausbeute 164.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
COc1ccc2c(c1)C(N(C)C)=CCC2
Reaction #367328
amber oil
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
COc1ccc(Oc2c(C)cc([N+](=O)[O-])cc2C)cc1C(=O)c1ccc(F)cc1
Reaction #406330
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
[O-2].[O-2].[O-2].[O-2].[O-2].[O]=[Ir].[Ta+5].[Ta+5]
Reaction #411324
iridium oxide tantalum oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
[O-2].[O-2].[O-2].[O-2].[O-2].[O]=[Ir].[Ta+5].[Ta+5]
Reaction #411326
iridium oxide tantalum oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
C=CC.C=CC1CCCCC1
Reaction #413572
Vinylcyclohexane Propylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
Nc1ccc(Cl)c(Cl)c1
Reaction #416410
3,4-dichloroaniline
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
C[N+](C)(C)CCO.NC(N)=O.[Cl-]
Reaction #438493
Urea choline chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
N#C[C@H](O)c1ccccc1
Reaction #447096
(R)-(+)-α-cyanobenzyl alcohol
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
N#C[C@H](O)c1ccccc1
Reaction #447097
(R)-(+)-α-cyanobenzyl alcohol
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
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