benzyl 3-bromo-5-fluorophenyl ether

Oc1cc(F)cc(Br)c1
Reaction #48712
desired compound
المردود 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc(F)cc(OCc2ccccc2)c1
Reaction #48718
desired compound
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(C=Cc2cc(F)cc(OCc3ccccc3)c2)cc1
Reaction #166064
desired product
المردود 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)Oc1ccc(C=Cc2cc(F)cc(OCc3ccccc3)c2)cc1
Reaction #166066
desired product
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1ccc(C=Cc2cc(F)cc(OCc3ccccc3)c2)cc1
Reaction #181134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1(c2cc(F)cc(OCc3ccccc3)c2)CCOCC1
Reaction #181555
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1cc(F)cc(Br)c1
Reaction #230134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC1CCCC1(O)c1cc(F)cc(OCc2ccccc2)c1
Reaction #270968
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(O[Si](C)(C)C(C)(C)C)C(C)(O)c1cc(F)cc(OCc2ccccc2)c1
Reaction #336559
(2RS,3SR)-2-(3-benzyloxy-5-fluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-ol
المردود 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
Fc1cc(OCc2ccccc2)cc(-c2ccncc2)c1
Reaction #392195
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(O[Si](C)(C)C(C)(C)C)C(C)(O)c1cc(F)cc(OCc2ccccc2)c1
Reaction #741735
(2RS,3SR)-2-(3-benzyloxy-5-fluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-ol
المردود 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_07
O=Cc1cc(F)cc(OCc2ccccc2)c1
Reaction #751108
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)C=Cc1cc(F)cc(OCc2ccccc2)c1
Reaction #796863
methyl 3-(3-(benzyloxy)-5-fluorophenyl)acrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCC(O)(c1cc(F)cc(OCc2ccccc2)c1)c1nccs1
Reaction #828976
title product
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
COC1CCCC1(O)c1cc(F)cc(OCc2ccccc2)c1
Reaction #1117517
1-(3-benzyloxy-5-fluorophenyl)-2-methoxycyclopentanol
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
CC(=O)Oc1ccc(C=Cc2cc(F)cc(OCc3ccccc3)c2)cc1
Reaction #1202223
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Oc1cc(F)cc(Br)c1
Reaction #1333836
sub-title compound
المردود 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
OC1(c2cc(F)cc(OCc3ccccc3)c2)CCOCC1
Reaction #1464774
title compound
المردود 29.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
CCC(O)CO[Si](C)(C)C(C)(C)C
Reaction #1551089
tert-butyldimethylsilyloxybutan-2-ol
المردود 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_04
COC1CCCC1(O)c1cc(F)cc(OCc2ccccc2)c1
Reaction #1674562
1-(3-benzyloxy-5-fluorophenyl)-2-methoxycyclopentanol
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_06
الصفحة 1التالي