benzyl acrylate

Nc1ccc(/C=C/C(=O)OCc2ccccc2)cn1
Reaction #46486
title compound
المردود 39.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCOc2cc(/C=C/C(=O)O)cnc21
Reaction #46497
title compound
المردود 94.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CNC(=O)c1ncc(C=CC(=O)OCc2ccccc2)cn1
Reaction #181046
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(C=CC(=O)OCc2ccccc2)cn1
Reaction #224564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)C1CC(C(=O)OCc2ccccc2)C(c2ccccc2)N1
Reaction #228932
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)NC1CCN(CCC(=O)OCc2ccccc2)CC1
Reaction #242326
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)C1(CCC(=O)OCc2ccccc2)CCCCC1=O
Reaction #253205
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CCNCc1ccccc1)OCc1ccccc1
Reaction #300233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ccc(/C=C/C(=O)OCc2ccccc2)cn1
Reaction #313020
title compound
المردود 39.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)OC(=O)N1CCOc2cc(/C=C/C(=O)O)cnc21
Reaction #313027
title compound
المردود 94.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)OC(=O)N1CCCc2cc(/C=C/C(=O)OCc3ccccc3)cnc21
Reaction #313030
title compound
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)OC(=O)N1CCCc2cc(C=CC(=O)OCc3ccccc3)cnc21
Reaction #370070
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(CCN1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2F)CC1)OCc1ccccc1
Reaction #385699
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1ccc(C=CC(=O)OCc2ccccc2)cn1
Reaction #389963
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(CCNNC(=O)c1ccccc1)OCc1ccccc1
Reaction #451045
259
المردود 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CC(=O)C1(CCC(=O)OCc2ccccc2)CCCCC1=O
Reaction #461524
title compound
المردود 100.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
C=C(CCC(=O)OCc1ccccc1)C(=O)OCc1ccccc1
Reaction #486890
1
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
O=C(OCc1ccccc1)C1CC2C=CC1C2
Reaction #594908
title compound
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C(OCc1ccccc1)C1CC2C=CC1C2
Reaction #594913
title compound
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C(C=CCCC(CO)c1ccc(Br)cc1)OCc1ccccc1
Reaction #602570
title compound
المردود 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
الصفحة 1التالي