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CCOC(=O)C.C(Cl)Cl

CC(=O)OCc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4535
3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4536
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccccc2)OC(=O)C(Cl)(Cl)C(C(Cl)(Cl)Cl)N1OC(=O)Nc1ccccc1
Reaction #54970
product
Выход 39.0%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
Выход 94.0%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
Выход 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
Выход 79.5%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
Выход 42.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(C(=O)OCc1ccccc1C=C(Cl)Cl)c1ccc(Cl)cc1
Reaction #93197
2-(2,2-dichlorovinyl)-benzyl 2-(4-chlorophenyl)-isovalerate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(OC(=O)C1C(C=C(Cl)Cl)C1(C)C)c1ccccc1Cc1ccccc1
Reaction #95402
2,2-Dimethyl-3-(2',2'-dichlorovinyl)-cyclopropanecarboxylic acid 2benzyl-(α-vinyl)-benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1
Reaction #177848
DOI: 10.1039/C8SC04228D
CC(C)(CC=C(Cl)Cl)CC(=O)O
Reaction #178186
DOI: 10.1039/C8SC04228D
CC(=O)OC1C(COCc2ccccc2)OC(OC(=N)C(Cl)(Cl)Cl)C(OC(C)=O)C1OC(C)=O
Reaction #179800
DOI: 10.1039/C8SC04228D
CC(C)C(CC=C(Cl)Cl)C(=O)O
Reaction #179959
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC2C3CCC4CC(OC(C)=O)C(OCC)CC4(C)C3C(NC(=O)OCC(Cl)(Cl)Cl)CC12C
Reaction #181349
DOI: 10.1039/C8SC04228D
CC(=O)C(=NOCC(=O)OCC(Cl)(Cl)Cl)C(=O)OC(C)(C)C
Reaction #183281
DOI: 10.1039/C8SC04228D
CCOC(=O)C1C(C=C(Cl)Cl)C1(C)C
Reaction #184142
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)CCN(C(=O)C(Cl)Cl)c1ccnc(-c2cc(-c3c(Cl)cccc3Cl)no2)c1
Reaction #191562
DOI: 10.1039/C8SC04228D
CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1
Reaction #195539
DOI: 10.1039/C8SC04228D
CC1(C)[C@H](C=C(Cl)Cl)[C@@H]1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1
Reaction #213864
α-cyano-3-phenoxybenzyl cis-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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