子结构搜索

15024

O=C1c2ccccc2C(=O)N1OCc1ccccc1CBr
Reaction #9049
title compound
收率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47126
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47127
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47128
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C(=O)O)cc1
Reaction #47129
4-carboxybenzaldehyde
收率 95.6%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C(=O)O)cc1
Reaction #47130
4-carboxybenzaldehyde
收率 74.4%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C(=O)O)cc1
Reaction #47131
4-carboxybenzaldehyde
收率 70.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47132
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(ON1C(=O)c2ccccc2C1=O)c1ccccc1
Reaction #47133
N-benzoyloxyphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1
Reaction #47135
benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccccc1
Reaction #47136
acetophenone
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1
Reaction #47137
benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1
Reaction #47138
benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1
Reaction #47139
benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CSCCCON1C(=O)c2ccccc2C1=O
Reaction #49007
2-(3-methylsulfanyl-propoxy)-isoindole-1,3-dione
收率 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)CON
Reaction #49017
2-aminooxy-N-propyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC(=O)CON
Reaction #49018
2-aminooxy-N-isopropyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCON1C(=O)c2ccccc2C1=O
Reaction #49025
4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
NP([O-])ON1C(=O)c2ccccc2C1=O.OC[C@@H]1CC(O)CN1
Reaction #49185
compound 45a
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C1CCNC1.NP([O-])ON1C(=O)c2ccccc2C1=O
Reaction #49202
compound 78
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
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