مشارك في 31 تفاعل

COC(=O)C1(N)CCCCC1

COC(=O)C1(NC(=O)OCc2ccco2)CCCCC1
Reaction #161007
title compound
المردود 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1(C(=O)O)CCCCC1)N1CCSC1
Reaction #161014
title compound
المردود 66.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C1(NC(=O)c2ccc(-c3csc(N4CCN(N5CCOCC5)CC4)n3)cc2)CCCCC1
Reaction #161051
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C1(NS(=O)(=O)c2ccc(OC)cc2)CCCCC1
Reaction #210107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C1(NC(=O)c2ccoc2)CCCCC1
Reaction #288844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C1(N)CCCCC1
Reaction #372549
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)C1(NC(=O)c2sccc2C)CCCCC1
Reaction #372852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)C1(NC(=O)OCc2ccco2)CCCCC1
Reaction #535912
title compound
المردود 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(NC1(C(=O)O)CCCCC1)N1CCSC1
Reaction #535920
title compound
المردود 66.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COC(=O)C1(NC(=O)c2ccc(-c3csc(N4CCN(N5CCOCC5)CC4)n3)cc2)CCCCC1
Reaction #535958
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COC(=O)C1(NS(=O)(=O)c2ccc3c(Cl)cnc(Cl)c3c2)CCCCC1
Reaction #761339
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)C1(NC(=O)c2ccc(-c3csc(N4CCN(N5CCOCC5)CC4)n3)cc2)CCCCC1
Reaction #891775
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)C1(NC(=O)c2ccc(OC)cc2)CCCCC1
Reaction #1025531
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC#CCOc1ccc(S(=O)(=O)NC2(C(=O)OC)CCCCC2)cc1
Reaction #1046899
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)C1(N)CCCCC1
Reaction #1227526
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COC(=O)C1(N)CCCCC1
Reaction #1496725
methyl 1-amino-cyclohexanecarboxylate
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
COC(=O)C1(N)CCCCC1
Reaction #1633153
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COC(=O)C1(NCC(C)(NC(=O)OC(C)(C)C)c2cc(F)cc(F)c2)CCCCC1
Reaction #1638478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COC(=O)C1(NC(=O)c2ccc(CCl)cc2)CCCCC1
Reaction #1643801
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COC(=O)C1(NC(=O)OCc2ccco2)CCCCC1
Reaction #1714627
title compound
المردود 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
الصفحة 1التالي