4-hydroxy-4'-nitrobiphenyl

C=CCCCOc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #62967
4-(4-Penteneoxy)-4'-nitrobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=[N+]([O-])c1ccc(-c2ccc(OCCCCCCO)cc2)cc1
Reaction #62969
4-(6-Hydroxyhexyloxy)-4'-nitrobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(C)N(C(=O)COc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1)C(C)C
Reaction #231716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccc(-c2ccc(OCCCCCCO)cc2)cc1
Reaction #319368
4-(6-Hydroxyhexyloxy)-4'-nitrobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
O=[N+]([O-])c1ccc(-c2ccc(OCCCCCCBr)cc2)cc1
Reaction #319371
4-(6-Bromohexyloxy)-4'-nitrobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
O=[N+]([O-])c1ccc(-c2ccc(OC3CN4CCC3CC4)cc2)cc1
Reaction #399969
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)N(C(=O)COc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1)C(C)C
Reaction #487437
expected product
المردود 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
COC(=O)COc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #580695
(4′-nitro-biphenyl-4-yloxy)-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
COC(=O)C(Cc1ccccc1)Oc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #580697
2-(4′-nitro-biphenyl-4-yloxy)-3-phenyl-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(O)c1ccc(COc2ccc(-c3ccc([N+](=O)[O-])cc3)cc2)o1
Reaction #730979
5-(4′-Nitro-biphenyl-4-yloxymethyl)-furan-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=[N+]([O-])c1ccc(-c2ccc(OC3CN4CCC3CC4)cc2)cc1
Reaction #769409
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCOc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #943179
title compound
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
O=C(O)c1ccc(COc2ccc(-c3ccc([N+](=O)[O-])cc3)cc2)o1
Reaction #986705
5-(4′-Nitro-biphenyl-4-yloxymethyl)-furan-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CC(C)(C)OC(=O)C(C)(C)Sc1nc(CCOc2ccc(-c3ccc([N+](=O)[O-])cc3)cc2)cs1
Reaction #1001700
title compound
المردود 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
O=[N+]([O-])c1ccc(-c2ccc(OC3CN4CCC3CC4)cc2)cc1
Reaction #1057155
3-[(4′-nitro-1,1′-biphenyl-4-yl)oxy]quinuclidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
C=CCCCOc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #1175608
4-(4-Penteneoxy)-4'-nitrobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
O=[N+]([O-])c1ccc(-c2ccc(OC3CN4CCC3CC4)cc2)cc1
Reaction #1221092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C(O)c1ccc(COc2ccc(-c3ccc([N+](=O)[O-])cc3)cc2)o1
Reaction #1263962
5-(4′-Nitro-biphenyl-4-yloxymethyl)-furan-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
C=CCCCOc1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #1280641
4-(4-Penteneoxy)-4'-nitrobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_03
CC(C)(C)OC(=O)C(C)(C)Sc1nc(CCOc2ccc(-c3ccc([N+](=O)[O-])cc3)cc2)cs1
Reaction #1295775
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
الصفحة 1التالي