Busqueda de Subestructura

212687

COc1cc2c(c3c1c(=O)c1cc4ccccc4nc1n3C)[C@H]1OC(=O)O[C@H]1C(C)(C)O2
Reaction #46315
(±)-cis-7-Methoxy-4,4,15-trimethyl-15,15c-dihydro-4H-benzo[b][1,3]-dioxolo[4′,5′:3,4]chromeno[6,5-g][1,8]naphthyridin-2,8[3aH]-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(c2ccc(F)cc2)C(Cn2cncn2)(c2ccc(Cl)cc2Cl)O1
Reaction #93299
4-(2,4-dichlorophenyl)-5-(4-fluorophenyl)-2-oxo-4-(1H-1,2,4-triazol-1-yl)methyl-1,3-dioxolane
Rendimiento 78.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(c2ccc(F)cc2)C(Cn2cncn2)(c2ccc(Cl)cc2Cl)O1
Reaction #93300
4-(2,4-dichlorophenyl)-5-(4-fluorophenyl)-2-oxo-4-(1H-1,2,4-triazol-1-yl)methyl-1,3-dioxolane
Rendimiento 51.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(c2ccc(Cl)cc2)C(Cn2cncn2)(c2ccc(Cl)cc2Cl)O1
Reaction #93303
5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-2-oxo-4-(1H-1,2,4-triazol-1-yl)methyl-1,3-dioxolane
Rendimiento 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC1COC(=O)O1
Reaction #310498
1,2-butylene carbonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC=CCC=CCCCCCCCCC1(CCCCCCCC=CCC=CCCCCC)OC(=O)OC1CCCCCCCC=CCC=CCCCCC
Reaction #395708
DOI: 10.1039/C8SC04228D
Cn1nccc1[C@@]12CCCC[C@@H]1OC(=O)O2
Reaction #425207
title compound
Rendimiento 86.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1[C@@H]1CCCC[C@@H]1O
Reaction #425208
title compound
Rendimiento 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1[C@]12CCCC[C@H]1OC(=O)O2
Reaction #425211
title compound
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1[C@H]1CCCC[C@H]1O
Reaction #425212
title compound
Rendimiento 22.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2Cc3ccc(C(=O)N(C)C[C@H](O)[C@H]4OC(=O)O[C@@H]4[C@H](O)CO)n3Cc3ccccc32)ccc1C1=CCCCC1
Reaction #576762
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(OCc3ccccc3)c(C3OC(=O)OC3C[C@H]3CC[C@H](NC(=O)OC(C)(C)C)CC3)c2n1
Reaction #720985
{trans-4-[5-(3-benzyloxy-6-methoxy-[1,5]naphthyridin-4-yl)-2-oxo-[1,3]dioxolan-4-ylmethyl]-cyclohexyl}-carbamic acid tert-butyl ester
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(O)c(CC(O)C[C@H]3CC[C@H](NC(=O)OC(C)(C)C)CC3)c2n1
Reaction #720986
{trans-4-[2-hydroxy-3-(3-hydroxy-6-methoxy-[1,5]naphthyridin-4-yl)-propyl]-cyclohexyl}-carbamic acid tert-butyl ester
Rendimiento 68.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1C2OC(=O)OC2C(Oc2ccc3cc(NC(C)=O)c(=O)oc3c2)OC1(C)C
Reaction #750970
DOI: 10.1039/C8SC04228D
CC(C)(O)C(O)c1nc(-c2ccc(F)cc2F)c(-c2ccc(=O)n(-c3c(F)cccc3F)c2)o1
Reaction #755674
DOI: 10.1039/C8SC04228D
CCOC(=O)C1OC(=O)OC1c1ccc(OCc2ccc(OC/C(=N\OC)c3ccccc3)cc2)cc1
Reaction #1009511
titled compound
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Sc1ccccc1)C(O)c1ccc(OCc2ccc(OC/C(=N\OC)c3ccccc3)cc2)cc1
Reaction #1009512
titled compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2CCCCC2O1
Reaction #1132455
Hexahydro-1,3-benzodioxol-2-one
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)OC1C(=O)NC(C(=O)c1ccc(=O)n(-c2c(F)cccc2F)c1)c1ccc(F)cc1F
Reaction #1232816
DOI: 10.1039/C8SC04228D
CCOC(C)(OCC)C(C)=O
Reaction #1335842
3,3-diethoxy-2-butanone
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1
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