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BrCCCCCCC1CCCC1

BrCCCCCCC1CCCC1
Reaction #9904
(6-bromo-hexyl)-cyclopentane
Выход 94.1%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN1CCC[C@H]1c1ccc[n+](CCCCCCC2CCCC2)c1.[Br-]
Reaction #9905
(S)-1-(6-cyclopentyl-hexyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt
Выход 54.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)C(=O)CC[C@@H]12
Reaction #50340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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
CC12C=CC(=O)C=C1C(Br)CC1C2CCC2(C)C(=O)CCC12
Reaction #235405
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2CCC3C(CCC4(C)C(C(C)=O)CCC34)C2(C)CC1Br
Reaction #236903
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCC2C3CCC4=CC(=O)CCC4(C)C3(Br)C(F)CC12C
Reaction #240015
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2CCC3C4CCC(C(C)=O)C4(C)CC(=O)C3C2(C)CC1Br
Reaction #259991
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(CCCCCCC2CCCC2)CO1
Reaction #279822
DOI: 10.1039/C8SC04228D
BrCCCCCCC1CCCC1
Reaction #284622
DOI: 10.1039/C8SC04228D
CC12CC(O)C3C(CCC4=CC(=O)CCC43C)C1CCC2=O
Reaction #292319
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2C3CC(Br)=C4CC(O)CCC4(C)C3CCC12C
Reaction #294948
DOI: 10.1039/C8SC04228D
CCOCO[C@]1(C(=O)COC(C)=O)[C@@H](C)C[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #343337
21-acetoxy-17α-ethoxymethoxy-11β-hydroxy-6α,16β-dimethyl-1,4-pregnadiene-3,20-dione
Выход 68.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(OC(C)=O)[C@@H](C)C[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #343338
17α,21-diacetoxy-11β-hydroxy-6α,16β-dimethyl-1,4-pregnadiene-3,20-dione
Выход 101.5%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
Выход 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](Br)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #366009
Cholesteryl Bromide
DOI: 10.6084/m9.figshare.5104873.v1
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