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784738

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@@]4(O)[C@@H](C2)N(C)CC[C@]314
Reaction #155379
Oxycodone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314.Cl
Reaction #171322
oxycodone HCl
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314.Cl
Reaction #171323
oxycodone HCl
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314.Cl
Reaction #171324
oxycodone HCl
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314
Reaction #306663
Oxycodone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314.Cl
Reaction #342025
oxycodone hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314
Reaction #420691
Oxycodone
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@H]3[C@H]1C5
Reaction #453464
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 #453465
Hydromorphone
DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@]12CCC(=O)[C@]3(C)Oc4c(OC)ccc5c4[C@@]31CCN(CC1CC1)[C@@H]2C5.Cl
Reaction #456185
17-(cydopropylmethyl)-4,5α-epoxy-3-methoxy-5-methyl-14-n-propyloxymorphinan-6-one hydrochloride
Ausbeute 55.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@]12CCC(=O)[C@]3(C)Oc4c(O)ccc5c4[C@@]31CCN(CC1CC1)[C@@H]2C5
Reaction #456186
17-(cyclopropylmethyl)-4,5α-epoxy-3-hydroxy-5-methyl-14-n-propyloxymorphinan-6-one
Ausbeute 70.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314
Reaction #490276
Oxycodone
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@H]3[C@H]1C5
Reaction #516184
Hydromorphone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(CC2CC2)CC[C@]314
Reaction #517886
target compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2[C@H](NC)CC[C@@]3(O)[C@H]1C5
Reaction #517888
13
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314
Reaction #541979
oxycodone
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=NO)CC[C@@]3(O)[C@H]1C5
Reaction #565201
6-Oximino-17-ally-4,5 α-epoxy-3, 14-dihydroxymorphinan
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(C)C(=NO)C[C@@]3(O)[C@H]1C5
Reaction #565202
6-Methyloximino-17-allyl-4,5 α-epoxy-3, 14-dihydroxymorphinan
DOI: 10.6084/m9.figshare.5104873.v1
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