Recherche de Sous-structure

CC(CCO)CCc1ccccc1

Cc1c(CC(=O)O)c(=O)oc2cc([C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)ccc12
Reaction #2779
4
Rendement 60.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2S(=O)(=O)c2ccc(C(CC3CCOCC3)C(=O)Nc3nccs3)cc21
Reaction #43267
2-(10-Methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)-N-thiazol-2-ylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2S(=O)(=O)c2ccc(C(CC3CCOCC3)C(=O)Nc3nc(CC(=O)O)cs3)cc21
Reaction #43268
{2-[2-(10-Methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)propionylamino]thiazol-4-yl}acetic Acid
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(NC(=O)C(CC2CCOCC2)c2ccc3c(c2)Nc2ccccc2S3(=O)=O)n1
Reaction #43275
2-(5,5-Dioxo-5,10-dihydrophenothiazin-2-yl)-N-(1-methyl-1H-pyrazol-3-yl)-3-(tetrahydropyran-4-yl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C(F)(F)F
Reaction #48762
trifluoroacetate
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@]1(O)C[C@H]2CN(CCc3c([nH]c4c(I)cccc34)[C@@](C(=O)OC)(c3cc4c(cc3OC)N(C)[C@H]3[C@@](O)(C(=O)OC)[C@H](OC(C)=O)[C@]5(CC)C=CCN6CC[C@]43[C@@H]65)C2)C1
Reaction #48763
12′-iodovinblastine
Rendement 112.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@](O)(CCc1ccccc1)CC(=O)O
Reaction #51732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(C(F)(F)CC(CC(O)CSc3ccccc3)C(=O)O)cc2)cc1
Reaction #52038
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](/C=C/[C@@H]1[C@@H](Cc2cccc(OCc3ccccc3)c2)[C@@H](COS(=O)(=O)c2ccc(C)cc2)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #67889
((1S,2S,3R,4R)-2-(3-(benzyloxy)benzyl)-4-(tert-butyldimethylsilyoxy)-3-((S,E)-3-(tert-butyldimethylsilyoxy)oct-1-enyl)cyclopentyl)methyl 4-methylbenzenesulfonate
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](CC[C@@H]1[C@@H](Cc2cccc(OCc3ccccc3)c2)[C@@H](COS(=O)(=O)c2ccc(C)cc2)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #67890
titled compound
Rendement 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](CC[C@@H]1[C@H]2Cc3cccc(O)c3C[C@H]2C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #67892
(1R,2R,3aS,9aS)-2,3,3a,4,9,9a-hexahydro-2-(tert-butyldimethylsilyoxy)-1-((S)-3-(tert-butyldimethylsilyoxy)octyl)-1H-cyclopenta[b]naphthalen-5-ol
Rendement 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(CC2CCC(=O)C2)c2cc3cccnc3[nH]2)cc1
Reaction #176397
DOI: 10.1039/C8SC04228D
CN1c2ccccc2S(=O)(=O)c2ccc(C(CC3CCOCC3)C(=O)Nc3nc(CC(=O)O)cs3)cc21
Reaction #176863
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(C(CC2CCOC2)C(=O)Nc2cnccn2)cc1Cl
Reaction #180565
DOI: 10.1039/C8SC04228D
CN(CC1(CC=O)CCc2ccccc21)C(=O)OC(C)(C)C
Reaction #181512
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(C(CC2CCOCC2)C(=O)CCC(=O)c2ccccn2)cc1
Reaction #187091
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CC1CCOCC1)c1ccc(S(C)(=O)=O)cc1
Reaction #187804
DOI: 10.1039/C8SC04228D
CN(C)C(=O)c1cc(-c2nccs2)[nH]c1C(CC1CCOCC1)c1ccc(S(=O)(=O)C2CC2)cc1
Reaction #188456
DOI: 10.1039/C8SC04228D
CC(C)(O)C(O)c1cnc(C(=O)CCC(=O)C(CC2CCOCC2)c2ccc(S(C)(=O)=O)cc2)s1
Reaction #193468
DOI: 10.1039/C8SC04228D
CC1(CC=O)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C2C=CCC2)C1=O
Reaction #193537
DOI: 10.1039/C8SC04228D
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