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102145

CSc1ccc(Cc2c(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)n[nH]c2C)cc1
Reaction #7482
3-(β-D-glucopyranosyloxy)-5-methyl-4-[(4-methylthiophenyl)methyl]-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](c2cc3c(CCc4ccccc4)cccc3s2)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #43685
title compound
Выход 30.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cc2cccc3cc([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)sc23)cc1
Reaction #43690
title compound
Выход 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(CCCN4CCC(O)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45526
title compound
Выход 26.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CC1CCCCO1)C(=O)O
Reaction #47309
(S)-2-t-butoxycarbonylamino-3-(tetrahydro-pyran-2-yl)-propionic acid
Выход 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cn1ccc(NC(=O)[C@H](CC2CCCCO2)NC(=O)OC(C)(C)C)n1
Reaction #47310
[(S)-1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-2-(tetrahydro-pyran-2-yl)-ethyl]-carbamic acid t-butyl ester
Выход 57.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)c2ccc(OC)c(O)c2)cc1O
Reaction #48271
3-hydroxy-N-(3-hydroxy-4-methoxyphenyl)-4-methoxybenzamide
Выход 41.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)NOCC2CCCCO2)cc1
Reaction #57442
white crystals
Выход 7.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(O)C1
Reaction #62539
menthol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCc2ccc(S(C)(=O)=O)cc2O1
Reaction #67309
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCc2ccc(O)cc2O1
Reaction #67314
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1nnc(Cc2cc([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)ccc2Cl)s1
Reaction #74476
title compound
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@H]21
Reaction #76282
lovastatin
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79374
compounds A
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1[nH]cc(C)c(=O)c1C
Reaction #80712
compound 6
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23c4c5ccc(O)c4O[C@H]2[C@@H](O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C=C[C@H]3[C@H]1C5
Reaction #82147
morphine-6-glucuronide
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C1CC[C@]23O[C@H]2CCOC3C1
Reaction #160802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)O)c(C)n1CC1CCCCO1
Reaction #165690
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(=O)C(C(=O)c2ccc(C(F)(F)F)cc2[N+](=O)[O-])C(=O)O1
Reaction #174844
DOI: 10.1039/C8SC04228D
CCCCNc1nc(N)c2[nH]c(=O)n(CC3CCCCO3)c2n1
Reaction #183324
DOI: 10.1039/C8SC04228D
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