部分構造検索

C=CC(=O)O

CCOC(=O)C1=C2COC=CN2C(C)=C(C(=O)OC)C1c1ccccc1Cl
Reaction #1349
title compound
収率 65.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5641
title compound
収率 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5642
title compound
収率 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5644
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)[O-]
Reaction #40270
acrylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CC=C(C(=O)OC(C)C)CC2)c2cccc(-c3ccc(Cl)cc3Cl)c2n1
Reaction #51831
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnnc1C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2S(=O)C1
Reaction #54319
benzhydryl 7-phenoxyacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate-1-oxide
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC=C
Reaction #54632
butadiene
DOI: 10.6084/m9.figshare.5104873.v1
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65627
title compound
収率 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65628
title compound
収率 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65630
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(c2ccccc2Cl)=NC1=Cc1ccccc1
Reaction #72717
desired compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc2ccccc2c(-c2ccccc2Cl)n1
Reaction #72718
desired product
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=CC(c2cccc(C(F)(F)F)c2)=NN(C(=O)OCC)C1N1CCOCC1
Reaction #81047
6-(4-morpholinyl)-3-[3-(trifluoromethyl)phenyl]-1,5(6H)-pyridazindicarboxylic acid diethyl ester
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnnc(-c2cccc(C(F)(F)F)c2)c1
Reaction #81048
6-[3-(trifluoromethyl)phenyl]-4-pyridazinecarboxylic acid ethyl ester
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=CC(c2cccc(C(F)(F)F)c2)=NN(C(=O)OCC)C1N1CCOCC1
Reaction #82923
6-(4-morpholinyl)-3-[3-(trifluoromethyl)phenyl]-1,5(6H)-pyridazindicarboxylic acid diethyl ester
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnnc(-c2cccc(C(F)(F)F)c2)c1
Reaction #82924
6-[3-(trifluoromethyl)phenyl]-4-pyridazinecarboxylic acid ethyl ester
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C(/C)C(=O)OCC=C(C)C
Reaction #93593
3-methyl-2-butenyl angelate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)CCOC(=O)/C(C)=C\C
Reaction #93594
3-methyl-3-butenyl Angelate
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C(/C)C(=O)OCC/C=C\CC
Reaction #93595
(Z)-3-Hexenyl Angelate
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ