90 件の反応に参加

C1CC2C(C1)O2

OC1CCCC1Nc1ccccc1
Reaction #54515
N-(2-hydroxycyclopentyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC1(C)CN(C2CCCC2O)c2cc(C#N)ccc2O1
Reaction #65397
6-cyano-3,4-dihydro-4-(2-hydroxycyclopentan-1-yl)-2,2-dimethyl-2H-1,4-benzoxazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
OC1CCCC1Oc1ccc(Oc2ccccc2)cc1
Reaction #75055
2-(4-phenoxyphenoxy)-cyclopentan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O[C@@H]1CCC[C@H]1Nc1ccc(Cl)c(Cl)c1
Reaction #94013
trans-2-(3,4-dichloroanilino)cyclopentanol
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O[C@@H]1CCC[C@H]1NCc1ccccc1
Reaction #168338
trans-2-(benzylamino)cyclopentanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[N-]=[N+]=NC1CCCC1O
Reaction #206876
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
—
Reaction #218071
isomeric mixture
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
[N-]=[N+]=NC1CCCC1O
Reaction #228367
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC1CCCC1c1ccccc1
Reaction #252950
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCCCC1CCCC1O
Reaction #265817
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
—
Reaction #315523
isomeric mixture
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
OC1CCCC1Nc1ccccc1
Reaction #324196
N-(2-hydroxycyclopentyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_06
Cc1cc(Nc2ncnc3ccc(O[C@@H]4CCC[C@H]4O)cc23)ccc1Oc1ccn2ncnc2c1
Reaction #327771
title compound
収率 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
OC1CCCC1Nc1ccccc1
Reaction #350312
N-(2-hydroxycyclopentyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
O=C(O)CS[C@@H]1CCC[C@H]1O
Reaction #362581
trans-[(2-Hydroxycyclopentyl)thio]acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CC(C)(C)c1cc(S[C@@H]2CCC[C@H]2O)cc(C(C)(C)C)c1O
Reaction #362585
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COc1cc(OC)cc(C2CCCC2O)c1
Reaction #368480
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)c1ccc(OC2CCCC2O)c(C(C)(C)C)c1
Reaction #386506
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)CN(C2CCCC2O)c2cc(C#N)ccc2O1
Reaction #388045
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1nccc1[C@H]1CCC[C@@H]1O
Reaction #424899
title compound
収率 21.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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