مشارك في 22 تفاعل

315302

CCCCCCCCCC(C)NC(=O)C=C(c1ccccc1)c1ccc([N+](=O)[O-])cc1
Reaction #94898
title compound
المردود 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
—
Reaction #94899
oil
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #95086
title product
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #95088
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #95089
title product
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCCC(C)NC(=O)[C@@H]1C[C@H]1c1ccc([N+](=O)[O-])cc1
Reaction #95094
trans-N-(1-Methyldecyl)-2-(4-nitrophenyl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #185277
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCC(C)NC(=O)C1CC1c1ccc([N+](=O)[O-])cc1
Reaction #258793
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCC(C)NC(=O)C=C(c1ccccc1)c1cccc([N+](=O)[O-])c1
Reaction #766412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #935684
title product
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #935686
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #935687
title product
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #935748
title product
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #935750
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #935751
title product
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #1153000
title product
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_05
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #1153002
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_05
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #1153003
title product
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_05
CCCCCCCCCC(C)NC(=O)[C@@H]1C[C@H]1c1ccc([N+](=O)[O-])cc1
Reaction #1153008
trans-N-(1-Methyldecyl)-2-(4-nitrophenyl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_05
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #1214364
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
الصفحة 1التالي