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CC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(C1)C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70403
3β-tert-butyldimethylsilyloxyandrostane-6,17-dione
Выход 75.0%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
Выход 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
Выход 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
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC1CCC2(C)C(C1)C(=O)CC1C3CCC(=O)C3(C)CCC12
Reaction #236546
DOI: 10.1039/C8SC04228D
CN(CCC(=O)OC1CCC2(C)C(C1)C(=NO)CC1C3CCC(=O)C3(C)CCC12)C(=O)OCc1ccccc1
Reaction #261840
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
CC12CCC3C(CC(=O)C4CC(OC(=O)CNC(=O)OCC5c6ccccc6-c6ccccc65)CCC43C)C1CCC2=O
Reaction #395682
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCNC(=O)OC1CCC2(C)C(C1)C(=O)CC1C3CCC(=O)C3(C)CCC12
Reaction #765363
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C(=O)OC2CCC3(C)C(C2)C(=O)CC2C4CCC(=O)C4(C)CCC23)CC1
Reaction #1023304
DOI: 10.1039/C8SC04228D
CC12CCC3C(CC(=O)C4CC(O)CCC43C)C1CCC2=O
Reaction #1033628
DOI: 10.1039/C8SC04228D
C[C@]12CC[C@H](OC(=O)CCN)CC1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.Cl
Reaction #1999837
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(C1)C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #1999910
3β-tert-butyldimethylsilyloxy-androstane-6,17-dione
Выход 75.0%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 #1999911
3β-hydroxyandrostane-6,17-dione
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](OC(=O)CNC(=O)OCC3c4ccccc4-c4ccccc43)CC1C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #1999912
3β-{2-[N-(9-fluorenylmethoxycarbonyl)]aminoacetoxy}androstane-6,17-dione
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCNC(=O)O[C@H]1CC[C@@]2(C)C(C1)C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #1999913
3β-[N-(2-tert-butoxycarbonylaminoethyl)-carbamoyloxy]androstane-6,17-dione
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H](OC=O)CC1C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #1999924
3α-formyloxyandrostane-6,17-dione
Выход 90.0%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 #1999925
3α-hydroxyandrostane-6,17-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)S[C@H]1CC[C@@]2(C)C(C1)C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #1999926
3β-acetylthioandrostane-6,17-dione
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
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