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CCCCCCCCC(=O)C

CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCc4cccc(CO[Si](C)(C)C(C)(C)C)c4)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6398
title compound
Выход 58.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O[Si](C)(C)C(C)(C)C)C2C)C(OC)CC3C)CC1OC
Reaction #6399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4cccc(C=O)c4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6401
title compound
Выход 31.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2O
Reaction #40292
Testosterone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N=[N+]=[N-])C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40601
38
Выход 87.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40602
39
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O[Si](C)(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42650
title compound
Выход 103.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42651
title compound
Выход 73.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)O[C@]1(C(=O)COC(C)=O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42652
title compound
Выход 62.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #55608
methyl-4-androstene-3-one-17-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OCC(=O)[C@@]1(OC(=O)CC)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(Cl)[C@@H](O)C[C@@]21C.CCCCCC
Reaction #56383
beclomethasone dipropionate n-hexane
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OCC(=O)[C@@]1(OC(=O)CC)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(Cl)[C@@H](O)C[C@@]21C.CCCCCC
Reaction #56384
beclomethasone dipropionate n-hexane
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C[C@@H]4O[C@@]45C[C@@H](O)CC[C@]35C)[C@@H]1CCC2=O
Reaction #70359
3β-hydroxy-5α,6α-epoxyandrostane-17-one
Выход 47115.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #71582
steroids
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(C(=O)O)cc4CC[C@H]3[C@@H]1CC[C@@H]2C(=O)c1ccccc1
Reaction #81724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(C(=O)O)cc4CC[C@H]3[C@@H]1CC[C@@H]2C(=O)c1ccccc1
Reaction #81725
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(C(=O)O)cc4CC[C@H]3[C@@H]1CC[C@@H]2C(=O)c1ccccc1
Reaction #81726
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(C(=O)O)cc4CC[C@H]3[C@@H]1CC[C@@H]2C(=O)C1CCCCC1
Reaction #81727
title compound
Выход 8200.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(C(=O)O)cc4CC[C@H]3[C@@H]1CC[C@@H]2C(=O)c1ccccc1
Reaction #81728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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