TEOS

CCO[Si](OCC)(OCC)C(F)=C(F)F
Reaction #12072
CF2═CFSi(OEt)3
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCO[Si](OCC)(c1c(F)c(F)c(F)c(F)c1F)c1c(F)c(F)c(F)c(F)c1F
Reaction #12073
di(pentafluorophenyl)diethoxysilane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCO[Si](OCC)(OCC)OCC.O
Reaction #44957
water TEOS
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C/C(=N\c1c(C(C)C)cccc1C(C)C)c1cc(C)cc(Br)c1O
Reaction #73706
yellowish solid
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(Br)c(O)c(/C(=N/c2c(C(C)C)cccc2C(C)C)c2ccccc2)c1
Reaction #73711
34
Ausbeute 69.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1cccc(C(C)C)c1N=C(c1ccccc1)c1cccc(Br)c1
Reaction #73730
title product 17
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=Nc1c(C(C)C)cccc1C(C)C)c1cccc(Br)c1
Reaction #73755
13
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(C(=Nc2c(C(C)C)cccc2C(C)C)c2cccc(Br)c2)cc1
Reaction #73759
title product
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CO[Si](CCC1CCC2OC2C1)(OC)OC
Reaction #74689
(3,4-epoxycyclohexyl)ethyltrimethoxysilane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCOC(=O)CC1CCc2c1[nH]c1ccc(OC)cc21
Reaction #91079
ethyl 2-(7-methoxy-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetate
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)CC1CCc2c1[nH]c1ccc(OC)cc21
Reaction #91080
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC[n+]1cc[nH]c1.Oc1ccccc1
Reaction #163391
ethylimidazolium phenol salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163392
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163393
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163394
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Si+4].[Ti+4]
Reaction #216566
titanium-silicon hydroxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCO[Si](OCC)(OCC)OC(=O)C(F)(F)F
Reaction #275891
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CNC1CC(c2c[nH]c3ccccc23)c2ccccc21
Reaction #293814
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)c1ccc2c(c1)C(=O)OC2=O
Reaction #324370
TMAN
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COCC(C)OC(C)=O
Reaction #340060
PGMEA
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
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