Poly(p-hydroxystyrene)

C=Cc1ccc(O)cc1.C=Cc1ccc(OC2CCCCO2)cc1
Reaction #2770
p-tetrahydropyranyloxystyrene p-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(C)OCC)cc1
Reaction #216545
desired product
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
C=Cc1ccc(C2CCCCO2)cc1.C=Cc1ccc(O)cc1
Reaction #216550
title compound
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(C)(C)C)cc1
Reaction #216551
p-tert-butoxystyrene p-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(C)OCCC2CCCCC2)cc1
Reaction #440865
desired compound
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(=O)OC(C)(C)C)cc1
Reaction #440866
p-hydroxystyrene p-(tert-butoxycarbonyloxy)-styrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
C=Cc1ccc(O)cc1.C=Cc1ccc(OC2CCCCO2)cc1
Reaction #518093
p-tetrahydropyranyloxystyrene p-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
C=Cc1ccc(O)cc1.C=Cc1ccc(OC2CCCCO2)cc1
Reaction #529786
p-hydroxystyrene p-(t-butyloxycarbonyloxy)styrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
C=Cc1ccc(O)cc1.C=Cc1ccc(OCC(=O)OC(C)(C)C)cc1
Reaction #831117
tert-butyl p-vinylphenoxyacetate p-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
C=Cc1ccc(O)cc1.C=Cc1ccc(OCC(=O)OC(C)(C)C)cc1
Reaction #831129
tert-butyl p-vinylphenoxyacetate p-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(=O)OC(C)(C)C)cc1
Reaction #1057445
p-hydroxystyrene p-tert-butoxycarbonyloxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(=O)OC(C)(C)C)cc1
Reaction #1106066
p-hydroxystyrene p-(tert-butoxycarbonyloxy)-styrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
COCC(C)OC(C)=O
Reaction #1114522
PGMEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COCC(C)OC(C)=O
Reaction #1114524
PGMEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COCC(C)OC(C)=O
Reaction #1114526
PGMEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COCC(C)OC(C)=O
Reaction #1114528
PGMEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(C)OCC)cc1
Reaction #1466073
desired product
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
C=Cc1ccc(C2CCCCO2)cc1.C=Cc1ccc(O)cc1
Reaction #1466078
title compound
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
C=Cc1ccc(O)cc1.C=Cc1ccc(OC(C)(C)C)cc1
Reaction #1466079
p-tert-butoxystyrene p-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
O=CC12CC=CCC1C1CC=CCC1O2
Reaction #1486656
PGMEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
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