compound ( 17 )

CC(OC(=O)NCCCS(=O)O)OC(=O)C(C)C
Reaction #317792
title compound ( 31 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(OC(=O)NCCCP(O)O)OC(=O)C(C)C
Reaction #405401
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
Reaction #476538
title compound ( 10 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
Reaction #476539
title compound ( 10 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
Reaction #476541
title compound ( 12 )
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
Reaction #617403
title compound ( 10 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
Reaction #617404
title compound ( 10 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
Reaction #617406
title compound ( 12 )
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(OC(=O)NCCCP(O)O)OC(=O)C(C)C
Reaction #632038
title compound ( 31 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(OC(=O)NCCCP(C)(=O)O)OC(=O)C(C)C
Reaction #632040
title compound ( 111 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(OC(=O)NCCCS(=O)O)OC(=O)C(C)C
Reaction #897402
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
Reaction #1000391
title compound
Yield 101.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
O=C(O)c1cccc(Cl)c1
Reaction #1036279
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C(O)c1cccc(Cl)c1
Reaction #1654247
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
Reaction #1763163
title compound ( 10 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
O=C(O)c1cccc(Cl)c1
Reaction #1763164
m-chlorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
Reaction #1763166
title compound ( 12 )
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
CC(OC(=O)NCCCP(O)O)OC(=O)C(C)C
Reaction #1814124
title compound ( 31 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
CC(OC(=O)NCCCP(C)(=O)O)OC(=O)C(C)C
Reaction #1814126
title compound ( 111 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
Reaction #1833534
title compound
Yield 101.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
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