bismuth(III) bromide

C#CCOC(C#N)c1ccc(Cl)cc1
Reaction #300328
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1c2ccccc2C(=O)N1[C@H]1CC[C@H](OCCc2ccccc2)CC1
Reaction #358509
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(C)CC=C(CO[C@H]1CC[C@H](N2C(=O)c3ccccc3C2=O)CC1)c1ccccc1
Reaction #358512
saturated product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCOC(=O)C1CCC(OCC2CC2)CC1
Reaction #773344
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
C#CCOC(C#N)c1ccc(Cl)cc1
Reaction #1180087
(4-chloro-phenyl)-prop-2-ynyloxy-acetonitrile
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCOC(=O)C1CC(OC2CCOCC2)CC1CC
Reaction #1207599
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COC(=O)c1ccc(C(C)OC)cc1
Reaction #1566908
methyl-4-(1-methoxyethyl)benzoate
المردود 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
COC(=O)c1ccc(C(C)OC(C)C)cc1
Reaction #1566911
methyl4-(1-isopropoxyethyl)benzoate
المردود 43.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CCOC(C)c1ccc(C(=O)OC)cc1
Reaction #1566914
methyl 4-(1-ethoxy ethyl)benzoate
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
COC(=O)c1ccc(C(C)OCC(C)C)cc1
Reaction #1566917
methyl 4-(1-isobutoxyethyl)benzoate
المردود 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CON(C)C(=O)[C@H]1CC[C@H](OCc2ccc(F)cc2)CC1
Reaction #1572285
titled compound
المردود 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
COC(=O)c1ccc(C(C)OC2CCCCC2)cc1
Reaction #1588355
methyl 4-(1-(cyclohexyloxy)ethyl)benzoate
المردود 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
CCCC1COC(c2ccc(OCc3ccccc3)c(F)c2)CC1Br
Reaction #1596944
2-(4-benzyloxy-3-fluorophenyl)-4-bromo-5-propyltetrahydropyran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
CCC1COC(c2ccc(Br)c(F)c2)CC1Br
Reaction #1596947
4-bromo-2-(4-bromo-3-fluorophenyl)-5-ethyltetrahydropyran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
O=C1c2ccccc2C(=O)N1[C@H]1CC[C@H](OCC2CC2)CC1
Reaction #1718614
12C
المردود 100.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CC(=O)OC[C@H]1O[C@H](Br)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #1860181
2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl bromide
المردود 100.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
CCCO[C@H]1CC[C@H](C(=O)OCC)CC1
Reaction #2056128
title compounds
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCO[C@H]1CC[C@H](N2C(=O)c3ccccc3C2=O)CC1
Reaction #2056148
title compound
المردود 42.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCOC(=O)C1CCC(OCC2CC2)CC1
Reaction #2056165
Ethyl 4-[(cyclopropylmethyl)oxy]cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCOC(=O)C1CC(OC2CCOCC2)CC1CC
Reaction #2056829
ethyl 2-ethyl-4-(tetrahydro-2H-pyran-4-yloxy)cyclopentanecarboxylate
المردود 140.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
الصفحة 1التالي