Поиск подструктуры

C[C@H](O)C(=O)O

CCOC(=O)c1oc2cccc(CCO)c2c1C
Reaction #57615
ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylate
Выход 80.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C(=O)OCC(Cl)(Cl)Cl)N2C(=O)C(NC(=O)Cc3ccccc3)[C@H]2S1=O
Reaction #346354
2,2,2-trichloroethyl 6-(2-phenylacetamido)-2,2-dimethylpenam-3-carboxylate-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C(=O)O)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2S1=O
Reaction #346356
6-(2-phenoxyacetamido)-2,2-dimethylpenam-3-carboxylic acid-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[O-].[Na+].[Na+]
Reaction #362819
sodium carbonate
DOI: 10.6084/m9.figshare.5104873.v1
CCP([O-])[O-].CCP([O-])[O-].CCP([O-])[O-].[Al+3].[Al+3]
Reaction #425230
ethylphosphonous acid aluminum(III) salt
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCP([O-])[O-].CCP([O-])[O-].CCP([O-])[O-].[Al+3].[Al+3]
Reaction #425231
ethylphosphonous acid aluminum(III) salt
Выход 95.9%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](Cc1ccccc1)N(C)C(=O)[C@@H](Cc1ccc2ccccc2c1)N(C)C(=O)C=CC1CN(C(=O)OC(C)(C)C)C1
Reaction #453364
title compound
Выход 64.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](N)(Cc1ccccc1)C(=O)NCC1CCCO1
Reaction #453367
(2R)-2-Methyl-amino-3-phenyl-N-((2-tetrahydrofuranyl)methyl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](Cc1ccccc1)N(C)C(=O)[C@@H](COCc1ccccc1)NC
Reaction #453372
(2R)-3-Benzyloxy-N-methyl-2-(methylamino)-N-((1R)-1-(methylcarbamoyl)-2-phenylethyl)propionamide
Выход 99.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](Cc1ccccc1F)NC
Reaction #453375
(2R)-3-(2-fluorophenyl)-N-methyl-2-(methylamino)-propionamide
Выход 67.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](Cc1ccccc1F)N(C)C(=O)[C@@H](Cc1ccc2ccccc2c1)NC
Reaction #453377
(2R)-N-((1R)-2-(2-fluorophenyl)-1-(methylcarbamoyl)ethyl)-N-methyl-2-methylamino-3-(2-naphthyl)propionamide
Выход 97.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](Cc1ccc(F)cc1)NC
Reaction #453381
(2R)-3-(4-fluorophenyl)-N-methyl-2-methylaminopropionamide
Выход 91.6%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](Cc1ccccc1)N(C)C(=O)[C@@H](Cc1ccc(-c2ccccc2)cc1)NC
Reaction #453384
(2R)-3-(1,1'-biphenyl-4-yl)-N-methyl-2-methylamino-N-((1R)-1-methylcarbamoyl-2-phenylethyl)propionamide
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(F)c(F)c1
Reaction #461800
3,4-difluorobenzoic acid
Выход 95.5%DOI: 10.6084/m9.figshare.5104873.v1
OO
Reaction #471744
hydrogen peroxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC(F)(F)F)ccnc1C[S+]([O-])c1nc2ccccc2[nH]1
Reaction #482007
lansoprazol
Выход 238.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCCOc1ccnc(C[S+]([O-])c2nc3ccccc3[nH]2)c1C
Reaction #482008
rabeprazol
Выход 200.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccnc(C[S+]([O-])c2nc3cc(OC(F)F)ccc3[nH]2)c1OC
Reaction #482009
pantoprazol
Выход 204.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc[nH]c(N=C(c2ccccc2)c2ccccc2)c1Cl
Reaction #495225
3-Chloro-2-(diphenylmethyleneamino)pyridin-4(1 H)-one
DOI: 10.6084/m9.figshare.5104873.v1
[NH4+].[OH-]
Reaction #515562
NH4OH
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее