Substructure Search

3978

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Reaction #5325
product
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@H](CC(=O)OC)OCc1ccccc1
Reaction #5717
methyl (R)-3-(benzyloxy)-tetradecanoate
Yield 112.8%DOI: 10.6084/m9.figshare.5104873.v1
O=CN1CC=C(c2ccc(N3C[C@H](CNc4ccon4)OC3=O)cc2F)CC1
Reaction #8239
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8240
solid
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2[nH]c(C(Cl)(Cl)Cl)nc2c1
Reaction #46790
methyl-2-trichloromethyl-1H-benzoimidazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2[nH]c(C(=O)NC3CCN(C(C)C)CC3)nc2c1
Reaction #46791
2-(1-isopropyl-piperidin-4-ylcarbamoyl)-1H-benzoimidazole-5-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2[nH]c(C(Cl)(Cl)Cl)nc12
Reaction #46794
Methyl-2-trichloromethyl-1H-benzoimidazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2[nH]c(C(=O)NC3CCN(C4CC4)CC3)nc2c1
Reaction #46854
2-(1-cyclopropyl-piperidin-4-ylcarbamoyl)-1H-benzoimidazole-5-carboxylic methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2[nH]c(C(=O)NC3CCN(C4CC4)CC3)nc2c1
Reaction #46898
2-(1-cyclopropyl-piperidin-4-ylcarbamoyl)-1H-benzoimidazole-5-carboxylic methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(=O)N1CC(=O)C(OCCCOC3C(=O)CN4C(=O)c5cc(OC)ccc5N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]34)[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)N2C(=O)OCC(Cl)(Cl)Cl
Reaction #47140
12
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(=O)N1C=C(OS(=O)(=O)C(F)(F)F)C(OCCCOC3C(OS(=O)(=O)C(F)(F)F)=CN4C(=O)c5cc(OC)ccc5N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]34)[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)N2C(=O)OCC(Cl)(Cl)Cl
Reaction #47141
triflate
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccccc1C1(OCCCOC2(c3ccccc3C#C)C=CN3C(=O)c4cc(OC)ccc4N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]32)C=CN2C(=O)c3cc(OC)ccc3N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]21
Reaction #47142
17
Yield 92.7%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccccc1C1(OCCCOC2(c3ccccc3C#C)C=CN3C(=O)c4cc(OC)ccc4N=C[C@H]32)C=CN2C(=O)c3cc(OC)ccc3N=C[C@H]21
Reaction #47143
glass
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(Cl)(Cl)Cl)N1CCc2ccc(S(=O)(=O)Cl)cc2C1
Reaction #51100
title compound ( D7 )
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #51103
2s
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C2CCN(C(=O)OCC(Cl)(Cl)Cl)CC2)c2ccccc21
Reaction #64890
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C2CCNCC2)c2ccccc21
Reaction #64891
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90568
306
Yield 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1[C@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90570
307
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC[C@H]1O[C@H](O[C@@H]2[C@H](OC(=O)c3ccccc3)[C@@H](O[C@@H]3[C@H](OC(=O)c4ccccc4)[C@@H](OCc4ccccc4)O[C@H](COC(=O)c4ccccc4)[C@H]3OC(=O)c3ccccc3)O[C@H](COC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162021
trisaccharide
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
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