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1406683

COC(=O)C(Oc1ccc(CBr)cc1)c1ccccc1Cl
Reaction #6021
Methyl 2-(4-bromomethylphenoxy)-2-(2'-chlorophenyl)acetate
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6560
boric acid ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(c2ccc(F)c(F)c2)Oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc2C1=O
Reaction #8898
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1c(-c2ccc(F)c(F)c2)oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #8899
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CCOCC1)C(O)(c1ccccc1)c1cccnc1
Reaction #50518
product
Выход 83.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)c1ccc(OCCO)cc1
Reaction #50779
4-(2-hydroxyethoxy)mandelic acid
Выход 89.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(O)C(=O)O)ccc1OCCO
Reaction #50780
4-(2-hydroxyethoxy)-3-methylmandelic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1ccc(C(O)C(=O)O)cc1
Reaction #50853
4-allyloxymandelic acid
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #65518
2.27
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Oc1ccc(CBr)cc1C(C)C)c1cccc(Cl)c1
Reaction #65522
title compound
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCOC(=O)C(Oc1cccc(C(F)(F)F)c1)c1ccc(Cl)cc1
Reaction #74262
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)(c1ccc(F)c(F)c1)c1ccc(F)c(F)c1
Reaction #77451
Ethyl 3,3′,4,4′-tetrafluorobenzilate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC)c1ccc(N)cc1
Reaction #84801
methyl 2-(4-aminophenyl)-2-methoxyacetate
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC)c1ccc(NS(=O)(=O)CCCCl)cc1
Reaction #84802
methyl 2-(4-(3-chloropropylsulfonamido)phenyl)-2-methoxyacetate
Выход 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(C(=O)O)c1cccc2ncccc12
Reaction #84806
2-methoxy-2-(quinolin-5-yl)acetic acid
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C(=O)N(C)OC)c1cccc2ncccc12
Reaction #84807
N,2-dimethoxy-N-methyl-2-(quinolin-5-yl)acetamide
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C(O)c1cc(F)cc2cccnc12
Reaction #94867
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164303
(R/S)-2-hydroxy-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetic acid
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCO)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164366
(R/S)-2-hydroxy-N-(2-hydroxyethyl)-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
Выход 68.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)CNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164367
(R/S)-2-hydroxy-N—((S)-2-hydroxypropyl)-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
Выход 47.1%DOI: 10.6084/m9.figshare.5104873.v1
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