Поиск подструктуры

741527

COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #1859
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(N)C(=O)O)cc1OCc1ccccc1
Reaction #5994
(RS)-4-Methoxy-3-(phenylmethoxy)phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C(NC(=O)COc2ccccc2)C1SSc1nc2ccccc2s1
Reaction #54380
2-[4-(benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid 2,2,2-trichloroethyl ester
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
N#Cc1cc(S(=O)(=O)Nc2ncns2)ccc1Oc1ccc(OC(F)(F)F)cc1-c1ccn[nH]1
Reaction #74521
title compound
Выход 46.9%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
NCCCC[C@H](NC(=O)OCC(Cl)(Cl)Cl)C(=O)O
Reaction #81366
(2,2,2-trichloroethoxycarbonyl)lysine
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #82192
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOc1ccc(C(=O)OCC(Cl)(Cl)Cl)o1
Reaction #85484
title compound
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
CC1(C)C2C(=O)OC(C(Cl)Cl)C21
Reaction #95556
desired product
Выход 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C2N=C(Cc3ccccc3)SC21)N1CCOCC1
Reaction #96110
2,2,2-trichloroethyl α-[3-benzyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholinoethylidene)acetate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCNC2CCC(C)(C)CC2)ccc1-c1cccc(C(N)=O)c1.O=C(O)C(F)(F)F
Reaction #157522
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N=C(OC1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H](O[C@H]2O[C@H](COC(=O)c3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](O[C@H]3O[C@H](COC(=O)c4ccccc4)[C@@H](OC(=O)c4ccccc4)[C@H](OC(=O)c4ccccc4)[C@@H]3OC(=O)c3ccccc3)[C@@H]2OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)C(Cl)(Cl)Cl
Reaction #162023
trichloroacetimidate
Выход 72.2%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(=O)OC1C(COCc2ccccc2)OC(OC(=N)C(Cl)(Cl)Cl)C(OC(C)=O)C1OC(C)=O
Reaction #179800
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCC(CC(=O)OC1C(NC(=O)OCC(Cl)(Cl)Cl)C(OCC2CCCN2C(=O)CC(CCCCCCCCCCC)OC(=O)CCCCCCCCC)OC(COC(=O)OC(C)(C)C(Cl)(Cl)Cl)C1OP(=O)(Oc1ccccc1)Oc1ccccc1)OC(=O)CCCCCCCCC
Reaction #181406
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
COC(=O)C1C(C=C(Cl)Cl)C1(C)C
Reaction #211716
DOI: 10.1039/C8SC04228D
Страница 1Далее