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43339

C[C@]12CC[C@H](O)CC1CC(=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70386
3β-hydroxyandrostane-7,17-dione
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1CC(=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70404
3β-hydroxyandrostane-6,17-dione
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)O[C@H]2CC[C@@]3(C)C(C2)C(=O)C[C@@H]2[C@@H]3CC[C@]3(C)C(=O)CC[C@@H]23)CC1
Reaction #70405
3β-(N-(tert-Butoxycarbonyl)piperidin-4-ylcarbonyloxy)androstane-6,17-dione
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C(=O)O[C@H]2CC[C@@]3(C)C(C2)C(=O)C[C@@H]2[C@@H]3CC[C@]3(C)C(=O)CC[C@@H]23)C1
Reaction #70406
3β-(N-(tert-Butoxycarbonyl)azetidin-3-ylcarbonyloxy)androstane-6,17-dione
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1CC[C@@]2(C)[C@@H](CC[C@@H]3[C@@H]2CC[C@]2(C)C(c4cccnc4)=CC[C@@H]32)C1
Reaction #81463
3α-Acetoxy-17-(3-pyridyl)-5α-androst-16-ene
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]12CCC[C@H]1[C@@H]1CC[C@H]3C[C@@H](O)CC[C@]3(C)[C@H]1CC2
Reaction #92527
5α-androstan-3β-ol
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O[C@H]2CC[C@@]3(C)[C@@H](CC[C@@H]4[C@@H]3CC[C@]3(C)C(=O)CC[C@@H]43)C2)cc1
Reaction #92528
3β-tosyloxy-5α-androstan-17-one
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12CC(=O)C3C(CCC4CC(O)CCC43C)C1CCC2=O
Reaction #176433
DOI: 10.1039/C8SC04228D
CC12CCC(O)CC1CCC1C2CCC2(C)C(N)C(O)CC12
Reaction #223775
DOI: 10.1039/C8SC04228D
CC12CCC3C(CCC4CC(O)CCC43C)C1CCC2=S
Reaction #228025
DOI: 10.1039/C8SC04228D
CC12CCC3C(CCC4CC5OC5CC43C)C1CCC2O
Reaction #230178
DOI: 10.1039/C8SC04228D
CC12CCC3C(CCC4CC(OCCO)CCC43C)C1CCC2=O
Reaction #240317
DOI: 10.1039/C8SC04228D
CC(C)(CNC(=O)OCc1ccccc1)C(=O)OC1CCC2(C)C(C1)C(=O)CC1C3CCC(=O)C3(C)CCC12
Reaction #282225
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(C(=O)OC2CCC3(C)C(C2)C(=O)CC2C4CCC(=O)C4(C)CCC23)C1
Reaction #293455
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)[C@@H](CC[C@@H]3[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]32)C1
Reaction #319977
titled compound
المردود 91.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC=CC[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #331425
desired compound 2
المردود 30.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H]3O[C@H]3CC1CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #331430
compound 22
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](N3CCNCC3)[C@@H](O)CC1CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #331431
compound 23
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #331432
compound 24
المردود 143.0%DOI: 10.6084/m9.figshare.5104873.v1
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