Recherche de Sous-structure

9350

COC1CCCCC1(O)c1cccnc1
Reaction #6004
(±)-2-methoxy-1-(pyrid-3-yl)cyclohexanol
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](O)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40591
8a
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40592
10
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40593
13
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40598
34
Rendement 81.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40599
35
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40604
10
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@H]3[C@H]1C5
Reaction #46033
Hydromorphone
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@H]3[C@H]1C5
Reaction #46034
Hydromorphone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@H]4[C@@H](C2)N(C)CC[C@]314.C[C@H](N)C(=O)N1CCC[C@H]1C(=O)O
Reaction #60610
solid
Rendement 675.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)O.COc1ccc2c3c1O[C@H]1C(=O)CC[C@H]4[C@@H](C2)N(C)CC[C@]314
Reaction #60611
solid
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)CNC(=O)CNC(=O)CNC(=O)CN)C(=O)O.COc1ccc2c3c1O[C@H]1C(=O)CC[C@H]4[C@@H](C2)N(C)CC[C@]314
Reaction #60613
solid
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC[C@@]2(O)[C@H]3Cc4ccc(O)c5c4[C@@]2(CCN3CC2CCC2)[C@H]1O5
Reaction #67604
N-(cyclobutylmethyl)-noroxymorphone
Rendement 73.2%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2c3c1O[C@H]1[C@@H](O)CC[C@@]4(O)[C@@H](C2)N(CC2CCC2)CC[C@]314
Reaction #67605
nalbuphine
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)C(O)CCC2CN(Cc3ccccc3)CC21
Reaction #83680
(3aRS,4RS,5RS,7aSR)-2-benzyl-4-(2-methoxyphenyl)-4,5-perhydroisoindolediol
Rendement 26.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCC2CN(Cc3ccccc3)CC2C1=O
Reaction #83681
(3aRS,5RS,7aSR)-5-acetoxy-2-benzyl-4-perhydroisoindolone
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
CC(=O)OC1CC(C)(C)C2CN(Cc3ccccc3)CC2C1=O
Reaction #83690
(3aRS,5RS,7aRS)-5 -acetoxy-2-benzyl-7,7-dimethyl-4-perhydroisoindolone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)C(O)CC(C)(c2ccccc2)C2CN(Cc3ccccc3)CC21
Reaction #83717
(3aRS,4RS,5RS,7SR,7aRS)-2-benzyl-7-methyl-7-phenyl-4-(2-methoxyphenyl)-4,5-perhydroisoindolediol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1OC1CCCCC1=O
Reaction #83828
ketone
Rendement 72.7%DOI: 10.6084/m9.figshare.5104873.v1
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