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334753

CCCCCCC(O)CCCCCCCCCCC(=O)NCCNCCO
Reaction #1215
title compound
Ausbeute 737.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1[C@@H](CC(=O)[O-])CC[C@H]1O
Reaction #2467
(1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Reaction #49204
amide
Ausbeute 93.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49205
Compound 83
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1(CC[C@@H]2[C@H](CC(=O)OC)[C@@H](O[SiH2]C(C)(C)C)C[C@H]2OC2CCCCO2)OCCO1
Reaction #50199
title compound ( 62 )
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
CC(C)C(=O)CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #56365
3α,6α-dihydroxy-5β-cholestan-24-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)C1=CC[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@]12C
Reaction #62998
21-acetoxy-11β-hydroxyl-1,4,16-pregnatriene-3,20-dione
Ausbeute 91.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C=CC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)C(C(=O)CC3CCCCO3)=CC[C@@H]12
Reaction #62999
21-tetrahydropyranyl-11β-hydroxy-1,4,16-pregnatriene-3,20-dione
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@@]43C)[C@@H]1C[C@@H](C#N)[C@@H]2C(=O)CC1CCCCO1
Reaction #63001
21-tetrahydropyranyl-16α-cyano-11β-hydroxy-3,20-dioxo-1,4-pregnadiene
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(N)C2CC3CC1CC(O)(C3)C2
Reaction #66726
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@]1(OC(C)=O)CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](OCOC)C[C@H](C)[C@]4(C)[C@H]3CC[C@@]21C
Reaction #95332
17β-acetoxy-3β-methoxymethoxy-1α-methyl-17α-n-propyl-5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(OCC(=O)O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162039
white solid
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)CC(=O)OC1CC2(C)C(C(C)=O)CCC2C2CCC3CC(OC=O)CCC3(C)C12
Reaction #180524
DOI: 10.1039/C8SC04228D
CC1(C)CN(C2CC3(C)C(CCC4C5CCC(C(=O)CSC#N)C5(C)CC(=O)C43)CC2O)CCO1
Reaction #184721
DOI: 10.1039/C8SC04228D
COc1ccc(CCC2(C3CCCC3)CC(=O)C(Cc3ccccc3)C(=O)O2)cc1Cl
Reaction #186143
DOI: 10.1039/C8SC04228D
CC12CCC(O)C=C1CCC1C2C(=O)CC2(C)C(C(=O)CBr)CCC12
Reaction #192455
DOI: 10.1039/C8SC04228D
CC12CCC(O)CC1CCC1C2CCC2(C)C(C(=O)COc3ccncc3)CCC12
Reaction #212328
DOI: 10.1039/C8SC04228D
CCCCCC(C=CC1C(OC2CCCCO2)CC2OC(C(Br)CCCC(=O)OC)CC21)OC1CCCCO1
Reaction #213779
DOI: 10.1039/C8SC04228D
COCC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)C=CC4(C)C3C(O)CC21C
Reaction #227101
DOI: 10.1039/C8SC04228D
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