90 件の反応に参加

C1CC2C(C1)O2

CCn1nccc1[C@H]1CCC[C@@H]1O
Reaction #424954
title compound
収率 16.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O[C@H]1CCC[C@@H]1c1ccnn1C1CCCCO1
Reaction #425135
title compound
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COc1cccc(C2CCCC2O)c1
Reaction #464487
1-hydroxy-2-(3-methoxyphenyl)-cyclopentane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
COc1cccc([C@@H]2CCC[C@H]2O)c1
Reaction #506081
titled compound
収率 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COc1cc(OC)cc([C@@H]2CCC[C@H]2O)c1
Reaction #506085
trans-2-(3,5-Dimethoxy-phenyl)-cyclopentanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
OC1CCCC1OC1CCCC1O
Reaction #517667
bis(2-hydroxycyclopentyl)ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
O[C@H]1CCC[C@@H]1c1cc(F)cc(F)c1
Reaction #538268
(1S,2R)-2-(3,5-difluorophenyl)cyclopentanol
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O[C@H]1CCC[C@@H]1c1cc(F)c(F)c(F)c1
Reaction #538273
(1S,2R)-2-(3,4,5-trifluorophenyl)cyclopentanol
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(OCc1ccccc1)N1CCN([C@@H]2CCC[C@H]2O)CC1
Reaction #554701
expected compound
収率 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O[C@H]1CCC[C@@H]1c1cc(F)cc(F)c1
Reaction #562983
(1S,2R)-2-(3,5-difluorophenyl)cyclopentanol
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O[C@H]1CCC[C@@H]1c1cc(F)c(F)c(F)c1
Reaction #562988
(1S,2R)-2-(3,4,5-trifluorophenyl)cyclopentanol
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
COc1ccccc1C1CCCC1O
Reaction #563044
2-(2-methoxyphenyl)cyclopentanol
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
—
Reaction #579679
isomeric mixture
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
OC1CCCC1OC1CCCC1O
Reaction #583159
bis(2-hydroxycyclopentyl) ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
OC1CCCC1n1cc(-c2ccc3cnc(Cl)cc3c2)cn1
Reaction #610242
title compound
収率 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
[N-]=[N+]=N[C@@H]1CCC[C@H]1O
Reaction #643835
desired product
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCCC1O
Reaction #786460
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
OCCN[C@@H]1CCC[C@H]1O
Reaction #805194
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O[C@@H]1CCC[C@H]1Cc1cc(F)cc(F)c1
Reaction #805203
trans-2-(3,5-difluorobenzyl)cyclopentanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
C[Si](C)(C)OC1CCCC1I
Reaction #916271
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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