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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
収率 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
収率 31.5%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
収率 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
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](NC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40603
40
収率 58.0%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
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](NS(C)(=O)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40605
42
収率 575.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](NS(=O)(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40606
43
収率 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCSCc1c(C)cc(C)c(C2CC(=O)C(C(CCC)=NOCC)=C(O)C2)c1C
Reaction #64059
5-[3-(n-Butylthiomethyl)-2,4,6-trimethylphenyl]-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)C1=C(O)CC(c2c(C)cc(O)cc2C)CC1=O
Reaction #64060
5-(2,6-dimethyl-4-hydroxyphenyl)-3-hydroxy-2-propionylcyclohex-2-en-1-one
収率 100.0%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
収率 47115.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](C(N)=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#C[C@H]1C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12
Reaction #70374
title compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@@H](C(=O)O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70401
7α-carboxyandrostane-3,17-dione
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12
Reaction #70402
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
収率 8200.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OC(=O)c4ccccc4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #83377
17-allyl-12-[2-(4-benzoyloxy-3-methoxycyclohexyl)-1-methyvinyl]-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CNC(=O)C1=C(O)c2ccc(C(F)(F)F)cc2C2(CCOCC2)C1=O
Reaction #174478
DOI: 10.1039/C8SC04228D
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