Cyclopentylacetic acid

NC(=O)CC1CCCC1
Reaction #1170
cyclopentylacetamide
수율 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@H](NC(=O)CC1CCCC1)C(=O)O
Reaction #51287
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)COC(=O)[C@H](C)NC(=O)CC1CCCC1
Reaction #51393
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)[C@H](C)NC(=O)CC1CCCC1
Reaction #51396
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=C(C)[C@@H]1CC[C@]2(NCCN3CCN(C(=O)CC4CCCC4)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172937
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)CN1C(=O)C(NC(=O)C(C)NC(=O)CC2CCCC2)C(=O)N(CC(C)C)c2ccccc21
Reaction #178455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(Cc1cccc(O)c1)NC(=O)CC1CCCC1
Reaction #213327
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)[C@H](C)NC(=O)CC1CCCC1
Reaction #220379
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)CN1C(=O)C(NC(=O)[C@H](C)NC(=O)CC2CCCC2)C(=O)N(CC(C)C)c2ccccc21
Reaction #220470
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C[C@H](NC(=O)CC1CCCC1)C(=O)C1(N)C(=O)N(CC2CC2)c2ccccc2N(CC2CC2)C1=O
Reaction #220473
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C[C@H](NC(=O)CC1CCCC1)C(=O)NC1C(=O)N(CC(C)(C)C)c2ccccc2N(CC(C)(C)C)C1=O
Reaction #220476
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C[C@H](NC(=O)CC1CCCC1)C(=O)NC1C(=O)N(c2ccccc2)c2ccccc2N(c2ccccc2)C1=O
Reaction #220479
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)COC(=O)[C@H](C)NC(=O)CC1CCCC1
Reaction #220578
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)[C@H](C)NC(=O)CC1CCCC1
Reaction #220581
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CN1CCN(c2cc(-c3ccc4c(c3)CN(C(=O)CC3CCCC3)CC4)nc(N)n2)CC1
Reaction #222523
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(O)c(-c2nn(C)cc2C#Cc2ccc(NC(=O)C3CCCCN3C(=O)C(Cc3ccccc3)NC(=O)CC3CCCC3)cc2)c1
Reaction #280609
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(CC1CCCC1)Nc1cccnc1SCCS(=O)(=O)c1cccc(C(F)(F)F)c1
Reaction #287924
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(Cl)CC1CCCC1
Reaction #312546
cyclopentylacetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
O=C(Cl)CC1CCCC1
Reaction #349099
cyclopentylacetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
COC(=O)c1ccc(Cc2cn(C)c3ccc(NC(=O)CC4CCCC4)cc23)c(OC)c1
Reaction #362325
title compound
수율 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
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