methyl 3-oxo-6-octenoate

CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #3099
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #82852
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC=CCCC(=O)CC(=O)OC
Reaction #567027
methyl 3-oxo-6-octenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #583939
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #931556
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #1051358
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #1078473
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_10
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #1359711
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #1363155
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_12
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #2248226
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)