مشارك في 18 تفاعل

1009015

COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #48394
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenyl azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48432
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #359091
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #359126
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #580807
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #580812
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #580845
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #588295
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #588333
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #1054723
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #1054761
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #1358664
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4c(Cl)cccc43)CC2)C1=O
Reaction #1358677
title compound
المردود 29.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #1453165
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #1453170
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #1453202
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #1855387
(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_06
COCCN1C[C@H](c2ccccc2)CC[C@@H](N)C1=O
Reaction #1855392
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_06