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COC(=O)C1CC2CCC1O2

O=C(O)C1C2CCC(O2)C1C(=O)OCc1ccccc1
Reaction #73454
10
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)C1C2CCC(O2)C1C(=O)N1CCN(CCO)CC1
Reaction #73455
3-[4-(2-hydroxy-ethyl)-piperazine-1-carbonyl]-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2C3CCC(O3)C12
Reaction #155664
product
Выход 50.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1OC(=O)C2=CC3CCCCC3C(O)C21
Reaction #192897
DOI: 10.1039/C8SC04228D
COC(=O)C1CC2CCC1O2
Reaction #210268
DOI: 10.1039/C8SC04228D
CC1OC(=O)C2=CC3CCCCC3C(O)C21
Reaction #229673
DOI: 10.1039/C8SC04228D
COC(=O)C1(NC(=O)c2ccc(OC)c(OCCc3cccc(C)c3)c2)CC2CCC1O2
Reaction #289654
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)NC2(C(=O)O)CC3CCC2O3)cc1OCCc1cccc(C)c1
Reaction #292907
DOI: 10.1039/C8SC04228D
COC(=O)C1C2CCC(O2)C1NCc1ccc(F)c(C)c1
Reaction #301169
DOI: 10.1039/C8SC04228D
O=C(O)C1C2CCC(O2)C1C(=O)OCc1ccccc1
Reaction #377818
DOI: 10.1039/C8SC04228D
COC(=O)C1(N)CC2CCC1O2
Reaction #397557
DOI: 10.1039/C8SC04228D
COC(=O)[C@H]1[C@@H](N)[C@@H]2CC[C@H]1O2
Reaction #511387
methyl (1R,2S,3R,4S)-3-amino-7-oxabicyclo[2.2.1]heptane-2-carboxylate
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1[C@@H](NCc2ccc(F)c(C)c2)[C@@H]2CC[C@H]1O2
Reaction #511388
methyl (1R,2S,3R,4S)-3-[(4-fluoro-3-methylbenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate
Выход 88.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CN2C(=O)C(C3=NS(=O)(=O)c4cc(NS(C)(=O)=O)ccc4N3)=C(O)[C@H]3[C@@H]2[C@@H]2CC[C@H]3O2)ccc1F
Reaction #511389
amide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1ccc2c(c1)S(=O)(=O)N=C(C1=C(O)[C@H]3[C@H]([C@@H]4CC[C@H]3O4)N(Cc3ccc(F)cc3)C1=O)N2
Reaction #511390
N-{3-[(1S,2R,7S,8R)-3-(4-fluoro-benzyl)-6-hydroxy-4-oxo-11-oxa-3-aza-tricyclo[6.2.1.02,7]undec-5-en-5-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl}-methanesulfonamide
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1[C@@H](N)[C@@H]2CC[C@H]1O2
Reaction #635495
methyl (1R,2S,3R,4S)-3-amino-7-oxabicyclo[2.2.1]heptane-2-carboxylate
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1[C@@H](NCc2ccc(F)c(C)c2)[C@@H]2CC[C@H]1O2
Reaction #635496
methyl (1R,2S,3R,4S)-3-[(4-fluoro-3-methylbenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate
Выход 88.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CN2C(=O)C(C3=NS(=O)(=O)c4cc(NS(C)(=O)=O)ccc4N3)=C(O)[C@H]3[C@@H]2[C@@H]2CC[C@H]3O2)ccc1F
Reaction #635497
amide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1ccc2c(c1)S(=O)(=O)N=C(C1=C(O)[C@H]3[C@H]([C@@H]4CC[C@H]3O4)N(Cc3ccc(F)cc3)C1=O)N2
Reaction #635498
N-{3-[(1S,2R,7S,8R)-3-(4-fluoro-benzyl)-6-hydroxy-4-oxo-11-oxa-3-aza-tricyclo[6.2.1.02,7]undec-5-en-5-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl}-methanesulfonamide
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1[C@H](NC(=O)OC(C)(C)C)[C@H]2CC[C@@H]1O2
Reaction #679234
desired compound
Выход 92.1%DOI: 10.6084/m9.figshare.5104873.v1
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