Recherche de Sous-structure

621262

CC(C)(C)OC(=O)NCC1CCN(CC(C)(C)C(=O)OCc2ccccc2)CC1
Reaction #44880
title compound
Rendement 1.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC(C)(C)C(=O)OCc3ccccc3)CC2)c2ccccc21
Reaction #44881
title compound
Rendement 67.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #61088
tert-butoxycarbonylamino-[4-(diethoxy-phosphoryl)-phenyl]-acetic acid benzyl ester
Rendement 93.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(OS(C)(=O)=O)C(NC(=O)OC(C)(C)C)C1
Reaction #84702
title compound
Rendement 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1[C@@H](Cc2ccc(C(F)(F)F)cc2)COC[C@H](NC(=O)c2nccc(OC)c2OCOC(=O)COCC)C(=O)O[C@H]1C
Reaction #87243
((4-methoxy-2-(((3S,7S,8R,9S)-9-methyl-2-oxo-8-propoxy-7-(4-(trifluoromethyl)benzyl)-1,5-dioxonan-3-yl)carbamoyl)pyridin-3-yl)oxy)methyl 2-ethoxyacetate
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(c1cccc(OC2CCCCO2)c1)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #95971
racemic 2-(tert-butoxycarbonylamino)-3-(3'-tetrahydropyranyloxyphenyl)-3-butenoic acid
Rendement 67.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cccc(N)c2)cc1)NC(=O)CCC(=O)OC
Reaction #158011
(R)-ethyl 4-(3′-aminobiphenyl-4-yl)-3-(4-methoxy-4-oxobutanamido)butanoate
Rendement 91.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cccc(NC(C)=O)c2)cc1)NC(=O)CCC(=O)OC
Reaction #158012
(R)-ethyl 4-(3′-acetamidobiphenyl-4-yl)-3-(4-methoxy-4-oxobutanamido)butanoate
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccccc1OC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #172573
ethyl 2-(2-(tert-butoxycarbonylamino)-3-phenylpropanoyloxy)benzoate
Rendement 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccccc1OC(=O)C(N)Cc1ccccc1
Reaction #172574
ethyl 2-(2-amino-3-phenylpropanoyloxy)benzoate
Rendement 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Sc1nc(CCOCc2ccc(-c3ccc(F)cc3)cc2)cs1)C(=O)O
Reaction #174588
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccc(N)c(Cl)c1)C(=O)OCc1ccccc1
Reaction #176160
DOI: 10.1039/C8SC04228D
CCOC(Cc1ccc(OCCN2CCOc3ccccc32)cc1)C(=O)O
Reaction #180008
DOI: 10.1039/C8SC04228D
NC(C=C(CCCO)CP(=O)(O)O)C(=O)O
Reaction #180100
DOI: 10.1039/C8SC04228D
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #180105
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)OC(OC(=O)C(O[Si](C)(C)C(C)(C)C)C(C)(C)COS(=O)(=O)CCCN=[N+]=[N-])C(C)C
Reaction #184808
DOI: 10.1039/C8SC04228D
CN(C)c1cc(NC(=O)OC(C)(C)C)c(NC(=O)CC(=O)c2cccc(-n3cc(COC4CCCCO4)cn3)c2)cc1C(F)(F)F
Reaction #190152
DOI: 10.1039/C8SC04228D
COc1ccc2ncc(F)c(CCCC3(C(=O)O)CCN(CCOc4c(F)cccc4F)CC3)c2c1
Reaction #194043
DOI: 10.1039/C8SC04228D
O=C(O)C1COCCN1Cc1ccccc1
Reaction #196798
DOI: 10.1039/C8SC04228D
COc1ccc2ncc(F)c(CCCC3(C(=O)O)CCN(CCOc4cc(F)c(F)c(F)c4)CC3)c2c1
Reaction #198745
DOI: 10.1039/C8SC04228D
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