部分構造検索

C=C(C)C(=O)O

C=C(C(=O)OCC)c1nc(CO)ccc1OCc1ccccc1
Reaction #1852
solution
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OCCCC)c1nc(CO)ccc1OCc1ccccc1
Reaction #1853
n-Butyl (3-benzyloxy-6-hydroxymethylpyridin-2-yl)propenoate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OC)c1nc(CO)ccc1OCc1ccccc1
Reaction #1854
product
収率 84.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)C(C[n+]2ccccc2)=C(O)O1.[OH-]
Reaction #5230
desired title product
収率 91.6%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OC)c1ccnc2ccc(OC)nc12
Reaction #43573
Methyl 2-[6-(methyloxy)-1,5-naphthyridin-4-yl]-2-propenoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1CCC(NC(=O)OC(C)(C)C)CC1)c1ccnc2ccc(OC)nc12
Reaction #43574
Methyl 3-[4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-1-piperidinyl]-2-[6-(methyloxy)-1,5-naphthyridin-4-yl]propanoate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OC)c1c(F)cnc2ccc(OC)nc12
Reaction #43590
product
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1CC[C@H](NC(=O)OCc2ccccc2)[C@H](F)C1)c1c(F)cnc2ccc(OC)nc12
Reaction #43611
Racemic methyl 2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]-3-[(cis)-3-fluoro-4-({[(phenylmethyl)oxy]carbonyl}amino)-1-piperidinyl]propanoate
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1CCO[C@@H](CNC(=O)OC(C)(C)C)C1)c1c(F)cnc2ccc(OC)nc12
Reaction #43620
Racemic methyl 3-{(2S)-2-[({[(1,1-dimethylethyl)oxy]carbonyl}amino)methyl]-4-morpholinyl}-2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]propanoate
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1CC[C@H](NC(=O)OC(C)(C)C)[C@H](OC)C1)c1c(F)cnc2ccc(OC)nc12
Reaction #43642
desired product
収率 142.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)NCCC(c2ccccc2)c2ccccc2)C(c2cccc(Cl)c2)N=C(N)N1
Reaction #52900
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CC[C@H](C=C(CC(=O)OCc2ccccc2)C(=O)OC(C)(C)C)CC1
Reaction #58040
trans-2-(4-tert-Butoxycarbonylamino-cyclohexylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl ester
収率 40.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CC[C@H](CC(CC(=O)O)C(=O)OC(C)(C)C)CC1
Reaction #58041
trans-2-(4-tert-Butoxycarbonylamino-cyclohexylmethyl)-succinic acid 1-tert-butyl ester
収率 110.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=C(C(=O)O)c2ccccc2)cc1
Reaction #59516
3-(4-Methoxyphenyl)-2-phenylacrylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(C(=O)O)c2ccccc2)cc1
Reaction #59517
3-(4-methoxyphenyl)-2-phenylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #64653
title compound
収率 60.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCSCC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #64654
title compound
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CNC(C(O)=NCc2ccccc2)C(C(=O)O)C1
Reaction #64980
5-Methyl-hexahydropyridine-2,3-dicarboxylic acid N-benzylimide
DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #65024
title compound
収率 60.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCSCC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #65025
title compound
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
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