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10323

CCOC(=O)c1cnc(CN2C(=O)c3ccccc3C2=O)c2c(OC)cc(OC)cc12
Reaction #42904
1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid ethyl ester
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(CN)c2c(OC)cc(OC)cc12
Reaction #42905
1-aminomethyl-6,8-dimethoxy-isoquinoline-4-carboxylic acid ethyl ester
Выход 123.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c2c(CN3C(=O)c4ccccc4C3=O)ncc(C(=O)O)c2c1
Reaction #42969
title compound
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2cnc(COC(C)=O)cc2OCc2ccccc2)cc1
Reaction #43435
oil
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2cnc(COC(C)=O)cc2C#C[Si](C)(C)C)cc1
Reaction #43605
desired compound
Выход 96.0%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
Выход 93.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2cc3ccc(C(F)(F)F)cc3c3cccc1c23
Reaction #64911
6-(Trifluoromethyl)phenanthrene-1,10-dicarboxylic Anhydride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Cc1cccc(C2(c3cccc(CC(C)(C)C(=O)OCC)c3)SCCCS2)c1
Reaction #76276
3-(3-{2-[3-(2-ethoxycarbonyl-2-methyl-propyl)-phenyl]-[1,3]dithian-2-yl}-phenyl)-2,2-dimethyl-propanoic acid ethyl ester
Выход 87.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)Cc1cccc(C2(c3cccc(CC(C)(C)CO)c3)SCCCS2)c1
Reaction #76277
3-(3-{2-[3-(3-hydroxy-2,2-dimethyl-propyl)-phenyl]-[1,3]dithian-2-yl}-phenyl)-2,2-dimethyl-propan-1-ol
Выход 85.9%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
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1ccc(N)cc1)C(=O)OCCOC(=O)C(C)Oc1ccc(N)cc1
Reaction #170985
32
Выход 72.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1ccc(N=C=O)cc1)C(=O)OCCOC(=O)COc1ccc(N=C=O)cc1
Reaction #170990
40
Выход 37.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #180105
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2(C#N)C3C=CC4C(C)(C)C(OC(=O)c5ccccc5)CCC4(C)C3CCC12C
Reaction #183662
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
COc1ccc(CCC2(C3CCCC3)CC(=O)C(Cc3ccccc3)C(=O)O2)cc1Cl
Reaction #186143
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)Cc1cccc(C2(c3cccc(CC(C)(C)C(=O)OCC)c3)SCCCS2)c1
Reaction #186254
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(CCc2ccc(F)cc2)nc2c(c1-c1cc(C(=O)NC3CCc4ccccc43)co1)C(=O)N1CCCC21
Reaction #191158
DOI: 10.1039/C8SC04228D
COc1ccc2ncc(F)c(CCCC3(C(=O)O)CCN(CCOc4c(F)cccc4F)CC3)c2c1
Reaction #194043
DOI: 10.1039/C8SC04228D
COc1ccc(N(C(=O)c2c3ccccc3nc3sccc23)S(=O)(=O)CCCC(=O)O)cc1
Reaction #194136
DOI: 10.1039/C8SC04228D
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