部分構造検索

CCOCC.ClCCl

C[C@@H]1Oc2ccccc2NC(=O)[C@H]1N.O=C(O)C(F)(F)F
Reaction #11690
(2S,3S)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1Oc2ccccc2NC(=O)[C@@H]1N.O=C(O)C(F)(F)F
Reaction #11691
(2S,3R)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt
DOI: 10.6084/m9.figshare.5104873.v1
CCOCCOc1cccc2[nH]c(C(Cl)(Cl)Cl)nc12
Reaction #46878
4-(2-Ethoxy-ethoxy)-2-trichloromethyl-1H-benzoimidazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1O[C@@H]1O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #48959
(2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2-oxo-2H-chromen-8-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(C[C@@H]1[C@H](C=C(Cl)Cl)C1(C)C)OC(C)=O
Reaction #55950
residue
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1Oc2ccccc2NC(=O)[C@H]1N.O=C(O)C(F)(F)F
Reaction #59415
(2S,3S)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1Oc2ccccc2NC(=O)[C@@H]1N.O=C(O)C(F)(F)F
Reaction #59416
(2S,3R)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=C(Cl)Cl)CC(=O)N1CCOCC1
Reaction #62057
2
収率 72927.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(Cl)oc(N2CCOCC2)c1
Reaction #62058
3
収率 75.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1
Reaction #75030
alpha-cyano-3-phenoxybenzyl 2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C/COC(=O)/C=C/c2ccc(O)c(OC)c2)ccc1O
Reaction #89788
coniferyl ferulate
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCC(=O)O[C@H]1[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #90566
212
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@@H]2[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](C)O[C@H]2O)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90567
318
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90568
306
収率 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1[C@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90570
307
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)C(C=C(Cl)Cl)=CS[C@H]12
Reaction #93024
benzhydryl 7-phenylacetamido-3-(2,2-dichlorovinyl)-2-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=C(Cl)Cl)CS(=O)[C@H]12
Reaction #93025
benzhydryl 7-phenylacetamido-3-(2,2-dichlorovinyl)-3-cephem-4-carboxylate-1-oxide
収率 42.6%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=C(Cl)Cl)CS[C@H]12)c1csc(NC=O)n1
Reaction #93029
benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(2,2-dichlorovinyl)-3-cephem-4-carboxylate
収率 67.5%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=C(Cl)Cl)CS[C@H]12)c1csc(N)n1
Reaction #93030
benzhydryl 7-[2-methoxyimino-2-(2-aminothiazol-4-yl)-acetamido]-3-(2,2-dichlorovinyl)-3-cephem-4-carboxylate
収率 93.9%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccccc1C=C(Cl)Cl
Reaction #93195
2-(2,2-Dichlorovinyl)-benzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1
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