Recherche de Sous-structure

OCC1CCN(Cc2ccccc2)C1

ClCC1CCN(Cc2ccccc2)C1
Reaction #961
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1[C@@H]1CN(Cc2ccccc2)C[C@H]1CO
Reaction #1166
expected product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@H]2CN(Cc3ccccc3)C[C@H]2CO)c(O)c1
Reaction #1167
expected product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1S(=O)(=O)OCC1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1986
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1CN(Cc2ccccc2)CC12CC2
Reaction #10440
title compound
Rendement 54.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(Cc2ccccc2)CCN(Cc2ccccc2)C1
Reaction #10458
title compound
Rendement 76.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1C(=O)N1CCC(CO)C1)OC/C=C/c1ccccc1
Reaction #62276
compound 74
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)CC(C)CC2CN(Cc3ccccc3)CC21
Reaction #83673
(3aRS,4RS,6SR,7aSR)-2-benzyl-4-(2methoxyphenyl)-6-methyl-4-perhydroisoindolol
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)CCCC2CNCC21
Reaction #83676
(3aRS,4RS,7aSR)-4-(2-methoxyphenyl)-4-perhydroisoindolol
Rendement 48.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)CCCC2CN(Cc3ccccc3)CC21
Reaction #83677
(3aRS,4RS,7aSR)-2-benzyl-4-(2-methoxyphenyl)-4-perhydroisoindolol
Rendement 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)C(O)CC(C)(C)C2CN(Cc3ccccc3)CC21
Reaction #83689
(3aRS,4RS,5RS,7aRS)-2-benzyl-7,7-dimethyl-4-(2-methoxyphenyl)-4,5-perhydroisoindolediol
Rendement 35.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)CCC(C)(CO)C2CNCC21
Reaction #83702
(3aRS,4RS,7SR,7aRS)-7-(hydroxymethyl)-4-(2-methoxyphenyl)-7-methyl-4-perhydroisoindolol
Rendement 56.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC2CCCCC12
Reaction #83705
perhydroisoindolone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cncn1NC(=O)C1CN(Cc2ccccc2)CC1C(F)(F)F
Reaction #85996
compound 13
Rendement 85.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(C(=O)O)CC2=O)c(OC)c1
Reaction #87166
1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acid
Rendement 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)N(Cc2ccc(OC)cc2OC)C1
Reaction #87167
methyl 1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylate
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C[C@H](C(=O)O)CC2=O)c(OC)c1
Reaction #87168
(R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acid
Rendement 90.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1(C(=O)O)CN(C(=O)c2ccc(F)cc2)CC1CCCB(O)O
Reaction #89668
racemic (3R,4S)-3-amino-4-[3-(dihydroxyboryl)propyl]-1-(4-fluorobenzoyl)pyrrolidine-3-carboxylic acid hydrochloride
Rendement 30.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170665
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C[C@@H](C(=O)N3C(=O)OC[C@H]3Cc3ccccc3)[C@H](C)C2=O)c(OC)c1
Reaction #170666
titled compound
Rendement 54.8%DOI: 10.6084/m9.figshare.5104873.v1
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