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294667

CCCCC[C@H]1CC[C@H](CCCOc2ccc(C=O)cc2)CC1
Reaction #64066
4-[3-(trans-4-pentylcyclohexyl)-1-propyloxy]benzaldehyde
収率 121.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](N3CCOCC3)[C@@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](C(=O)CBr)CC[C@@H]12
Reaction #64870
(2β,3α,5α)-21-bromo-3-hydroxy-2-(4-morpholinyl)pregnan-20-one
DOI: 10.6084/m9.figshare.5104873.v1
CC12CC(=O)C3C(CCC4CC(O)CCC43C)C1CCC2C(=O)CSCc1ccccc1
Reaction #188340
DOI: 10.1039/C8SC04228D
CC12CCC(O)C=C1CCC1C2C(=O)CC2(C)C(C(=O)CBr)CCC12
Reaction #192455
DOI: 10.1039/C8SC04228D
CC1CCC2(OC1)OC1CC3C4CCC5CC(=O)C=CC5(C)C4CCC3(C)C1C2C
Reaction #200852
DOI: 10.1039/C8SC04228D
CC12CCC(O)CC1CCC1C2CCC2(C)C(C(=O)COc3ccncc3)CCC12
Reaction #212328
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)CBr)C4(C)CCC3C2(C)C(OC(C)=O)C1
Reaction #234477
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2CCC3C(CCC4(C)C(C(C)=O)CCC34)C2(C)CC1Br
Reaction #236903
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(CCCOC2CCC(CCCCC)CC2)CC1
Reaction #248932
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2CCC3C4CCC(C(C)=O)C4(C)CC(=O)C3C2(C)CC1Br
Reaction #259991
DOI: 10.1039/C8SC04228D
COC1CC2(C)C(CCC3C4CCC(C(=O)COC(C)=O)C4(C)CC(=O)C32)CC1O
Reaction #271022
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(CCCOc2ccc(O)cc2)CC1
Reaction #273674
DOI: 10.1039/C8SC04228D
CC12CC(=O)C3C(CCC4CC(O)CCC43C)C1CCC2C(=O)CSc1ccccn1
Reaction #290708
DOI: 10.1039/C8SC04228D
C[C@]12CC[C@H](O)C[C@@H]1CC[C@H]1[C@@H]3CC[C@H](C(=O)CBr)[C@@]3(C)CC(=O)[C@@H]12
Reaction #320684
(3β,5α)-21-bromo-3-hydroxypregnane-11,20-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #320685
(3β,5α)-21-(acetyloxy)-3-hydroxypregnane-11,20-dione
収率 22.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)[C@@H](Br)C[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](Br)[C@@H](O)C[C@@H]1CC[C@H]1[C@@H]3CC[C@H](C#N)[C@@]3(C)CC(=O)[C@@H]12
Reaction #354803
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)C=C[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354805
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C=C[C@@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](C#N)CC[C@@H]12
Reaction #354809
title compound
収率 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCC2C3CCC4CC(=O)C(Br)C(C)C4(C)C3CCC12C
Reaction #370971
DOI: 10.1039/C8SC04228D
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