مشارك في 32 تفاعل

8613

O=C(O)CCc1ccc2c(c1)OCO2
Reaction #5121
3-(3,4-methylenedioxyphenyl) propanoic acid
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc2nc(N3CCN(C(=O)C=Cc4ccc5c(c4)OCO5)CC3)nc(N)c2cc1OC
Reaction #191917
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)CN(C(CCCCNC(=O)C=Cc1ccc2c(c1)OCO2)C(=O)O)S(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #235933
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN(CC)CC(C)(C)COC(=O)C=Cc1ccc2c(c1)OCO2.Cl
Reaction #355224
3-Diethylamino-2,2-dimethylpropyl 3,4-methylenedioxycinnamate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CCCn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(CCC)c1=O
Reaction #462472
Compound 18
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
CCn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(CC)c1=O
Reaction #462480
Compound 78
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
Cn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(C)c1=O
Reaction #462484
Compound 86
المردود 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
O=C(O)CCc1ccc2c(c1)OCO2
Reaction #769791
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(O)CCc1ccc2c(c1)OCO2
Reaction #1060966
3-(3,4-methylenedioxy-phenyl)-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11
CCCn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(CCC)c1=O
Reaction #1164634
Compound 19
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_08
CCn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(CC)c1=O
Reaction #1164667
Compound 87
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_08
Cn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(C)c1=O
Reaction #1164671
Compound 95
المردود 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_08
CCCn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(CCC)c1=O
Reaction #1168943
Compound 18
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
CCn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(CC)c1=O
Reaction #1168952
Compound 78
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
Cn1c(=O)c2[nH]c(/C=C/c3ccc4c(c3)OCO4)nc2n(C)c1=O
Reaction #1168956
Compound 86
المردود 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
Nc1ccccc1NC(=O)c1nc2c(s1)CN(C(=O)C=Cc1ccc3c(c1)OCO3)CC2
Reaction #1228345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C(O)CCc1ccc2c(c1)OCO2
Reaction #1331698
3-benzo-1,3-dioxol-5-ylpropionic acid
المردود 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
NC(=O)C=Cc1ccc2c(c1)OCO2
Reaction #1358575
3-Benzo[1,3]dioxol-5-yl-acrylamide
المردود 99.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
NC(=O)C=Cc1ccc2c(c1)OCO2
Reaction #1358599
3-Benzo[1,3]dioxol-5-yl-acrylamide
المردود 99.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
CC(C)CN([C@@H](CCCCNC(=O)C=Cc1ccc2c(c1)OCO2)C(=O)O)S(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #1369711
desired product
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
الصفحة 1التالي