部分構造検索

12047

CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #9621
ethyl 4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #9622
ethyl 4-(4′-amino-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)(CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C)C(=O)OCC
Reaction #9656
diethyl 2-[2-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)-2-oxoethyl]-2-(2-phenylethyl)malonate
収率 85.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C
Reaction #9657
ethyl 4-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #9658
solid
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #59115
ethyl 4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #59116
ethyl 4-(4′-amino-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)(CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C)C(=O)OCC
Reaction #59153
diethyl 2-[2-(3-methyl-4′-nitro-1,1′-biphenyl-4yl)-2-oxoethyl]-2-(2-phenylethyl)malonate
収率 85.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C
Reaction #59154
ethyl 4-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #59155
solid
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #250956
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCc1ccccc1)(CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C)C(=O)OCC
Reaction #391288
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #994844
ethyl 4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #994845
ethyl 4-(4′-amino-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)(CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C)C(=O)OCC
Reaction #994882
diethyl 2-[2-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)-2-oxoethyl]-2-(2-phenylethyl)malonate
収率 85.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C
Reaction #994883
ethyl 4-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #994884
solid
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1C
Reaction #1306426
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1C
Reaction #2247544
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #2402128
DOI: 10.1039/C8SC04228D
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