子结构搜索

C(CC=O)CC=O

CC(C)=O.CO.O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
Reaction #857
Citrate Acetone MeOH
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=O.CO.O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
Reaction #858
Citrate Acetone MeOH
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCO)CCO
Reaction #7102
3,3-dimethyl-1,5-pentanediol
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)c4cccs4)c3C2=O)C(=O)N1
Reaction #10069
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}-2-thienylcarboxamide
收率 47.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NCc4cccs4)c3C2=O)C(=O)N1
Reaction #10135
product
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)NC1=O
Reaction #42857
3,3-dimethylpiperidin-2,6-dione
收率 86.2%DOI: 10.6084/m9.figshare.5104873.v1
[Ag]
Reaction #43395
silver
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(O)(CC(=O)O)C(=O)[O-].[Ag+]
Reaction #43396
silver dihydrogen citrate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #46032
Citric Acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@](CCC(=O)O)(NC(C)=O)C(=O)O
Reaction #54312
N-acetyl-2-vinylglutamic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C12CC3CC(C1)C(=O)C(C3)C2
Reaction #66728
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CC3CC1CC(C(=O)O)(C3)C2
Reaction #66729
( 11 )
收率 91.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C12CC3CC(C1)C(N)C(C3)C2
Reaction #69977
4-aminoadamantane-1-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O.O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #70153
Citric acid monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(-c2ccc(C(=O)O)cc2)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #74184
4-[4-(2,4-dioxobicyclo[3.2.1]oct-3-yl)-5-methylthiophen-2-yl]benzoic acid
收率 77.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-].O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[NH4+].[NH4+].[NH4+]
Reaction #86691
triammonium citrate dextrose
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-].O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[NH4+].[NH4+].[NH4+]
Reaction #86692
solids
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-].O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[NH4+].[NH4+].[NH4+]
Reaction #86693
solids
收率 8.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-].O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[NH4+].[NH4+].[NH4+]
Reaction #86694
solids
收率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@@H](C(=O)O)CCC1=O
Reaction #87155
(S)-1-(tert-butoxycarbonyl)-6-oxopiperidine-3-carboxylic acid
收率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
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