子结构搜索

COC(C)=O

COC(=O)CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
Reaction #42135
title intermediate
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52263
solid
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52264
solid
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1cc2cc(OCCCNC(=O)NCc3ccccc3)ccc2[nH]1
Reaction #52265
title compound
收率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1cc2cc(OCCCNC(=O)NCc3ccccc3)ccc2[nH]1
Reaction #52266
title compound
收率 82.2%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
收率 93.1%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
收率 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
收率 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
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)OC(C)(C)C)C(=O)Oc1ccc(C2(c3ccccc3)CCCCC2)cc1
Reaction #157911
tert-Butyl 1-((4-(1-phenylcyclohexyl)phenoxy)carbonyl)-2-methylpropylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(N)C(=O)Oc1ccc(C2(c3ccccc3)CCCCC2)cc1
Reaction #157912
4-(1-Phenylcyclohexyl)phenyl 2-amino-3-methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1ccc(N)cc1)C(=O)OCCOC(=O)C(C)Oc1ccc(N)cc1
Reaction #170985
32
收率 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
收率 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
CN1C(=O)N(Cc2ccc(C(F)(F)F)cc2)CC1CCOc1ccc(CC(C)(C)C(=O)O)cc1
Reaction #183507
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
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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