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38719

Cc1cn([C@H]2C[C@H](ON)[C@@H](CO)O2)c(=O)[nH]c1=O
Reaction #82912
compound 4
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(OCc2ccccc2F)c2nc(C)c(C(=O)N[C@@H](CO)c3ccccc3)n2c1
Reaction #92738
ethyl 8-[(2-fluorobenzyl)oxy]-3-{[(1R)-2-hydroxy-1-phenylethyl]carbamoyl}-2-methylimidazo[1,2-a]pyridine-6-carboxylate
Выход 73.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1C(=O)[C@H](CO)[C@H]1S(=O)(=O)c1ccccc1
Reaction #93714
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(C(N)=O)c(NC(N)=O)[nH]c2c1
Reaction #303812
title compound
Выход 90.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2csc3cc4c(cc23)[C@]2(OC4)O[C@H](COCc3ccccc3)[C@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)cc1
Reaction #309120
titled compound
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(CCC(CO)(CCCCc1ccc(Sc2cccc(OCc3ccccc3)c2)cc1Cl)NC(=O)OC(C)(C)C)OC
Reaction #359472
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)CCCc1ccc2cc(CO)ccc2c1
Reaction #435920
compound
Выход 50.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C[C@@H]2N[C@@H](c3ccccc3)[C@@H](c3ccccc3)OC2=O)ccc1O
Reaction #457006
(2R, 3S, 5S)-6-oxo-2,3-diphenyl-5-(3-tert-butyl-4-hydroxybenzyl)morpholine
Выход 89.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)OCC(O)COC(=O)CCCCCCC/C=C\CCCCCCCC
Reaction #463604
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(c3cn4cncc4s3)[C@H](C)[C@H]12
Reaction #469790
4-nitrobenzyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-2-yl)-1-methyl-1-carbapen-2-em-3-carboxylate
Выход 64.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(O)c(Cl)c4C)c3)ccc21
Reaction #503352
title compound
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(C)c2ccc(O)cc2C)cc1C
Reaction #511991
title compound
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCN(CCCO)C2=O
Reaction #533733
title compound
Выход 145.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCC(=O)c1ccc(CO)cc1)C(=O)OC(C)(C)C
Reaction #533753
title compound
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C[C@H](C[C@H]1CC[C@H](O)CC1)NC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #538925
tert-butyl (S)-1-(trans-4-hydroxycyclohexyl)-3-(N-(benzyloxycarbonyl)-N-methylamino)propan-2-ylcarbamate
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](CO)CC1CCCC1
Reaction #538961
(S)-tert-butyl 1-cyclopentyl-3-hydroxypropan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(O)c(Cl)c4C)c3)ccc21
Reaction #540628
title compound
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ccc(-c2ccccc2)cc1NC(=O)c1cc(N2CCC(O)CC2)ccc1OCc1ccccc1
Reaction #541780
tert-butyl 2-(2-(benzyloxy)-5-(4-hydroxypiperidin-1-yl)benzamido)-4-phenylbenzoate
Выход 86.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2ccccc2)cc1NC(=O)c1cc(C2CCN(CCO)CC2)ccc1OCc1ccccc1
Reaction #541908
methyl 2-(2-(benzyloxy)-5-(1-(2-hydroxyethyl)piperidin-4-yl)benzamido)-4-phenylbenzoate
Выход 78.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(CCO)c2ccccc2C(c2ccccc2)N1C1CCN(Cc2cccc(CO)c2)CC1
Reaction #566643
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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