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CCCCCC1(CC[C@@H]2[C@@H](CC(O)C(F)(F)C#CCCO[Si](C)(C)C(C)(C)C)[C@@H](O[SiH2]C(C)(C)C)C[C@H]2OC2CCCCO2)OCCO1
Reaction #50200
title compound ( 65 )
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC(C)=O)CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CCC21OCCO1
Reaction #51637
3-acetate
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC2(C[C@@H]3CC[C@@H]4[C@H](CC[C@]5(C)C(=O)CC[C@@H]45)[C@@]13C)OCCO2
Reaction #95329
3,3-ethylenedioxy-1-methyl-5α-androstan-17-one
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1CCC2C3CCC4CC(O)C(C)CC4(C)C3C(=O)CC12C
Reaction #174790
DOI: 10.1039/C8SC04228D
CCCCCC(C)(O)C=CC1CCC2(OCCO2)C1CCCCCCCO
Reaction #188877
DOI: 10.1039/C8SC04228D
O=CC1CCC2(OCCO2)C1CCCCCCCO
Reaction #191854
DOI: 10.1039/C8SC04228D
CCCCCC(=O)C=CC1CCC2(OCCO2)C1C(CCCCC)C(=O)O
Reaction #201498
DOI: 10.1039/C8SC04228D
CC1(CCC23OC4CC5(C)C(=O)CCC5C(OCC2=O)C43)OCCO1
Reaction #202881
DOI: 10.1039/C8SC04228D
CC12CCC(O)CC1CCC1C2C(N)CC2(C)C1CCC21OCCO1
Reaction #210059
DOI: 10.1039/C8SC04228D
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC4(OCCO4)[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #213851
6,6-ethylenedioxy-5α-cholestan-3-one
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C1OCCO1)C1CCC2C3C=CC4=CC(O)C5OC5C4(C)C3CCC12C
Reaction #226081
DOI: 10.1039/C8SC04228D
CCCOCC(=O)C=CC1CCC2(OCCO2)C1CCCCCCCO
Reaction #227529
DOI: 10.1039/C8SC04228D
CC(=O)OCCCCCC1Cc2cc(OC(C)=O)ccc2C2CCC3(C)C(CCC34OCCO4)C12
Reaction #227987
DOI: 10.1039/C8SC04228D
N#CC1CCC2(OCCO2)C1CCCCCCCO
Reaction #241051
DOI: 10.1039/C8SC04228D
CC1(C2=CCC3C4CCC5CC(O)CCC5(C)C4C(=O)CC23C)OCCO1
Reaction #261438
DOI: 10.1039/C8SC04228D
CC12CCC3(CC1CCC1C2CCC2(C)C1CCC2(C)O)OCCO3
Reaction #264936
DOI: 10.1039/C8SC04228D
CC1CC2(CC3CCC4C5CCC(=O)C5(C)CCC4C13C)OCCO2
Reaction #271348
DOI: 10.1039/C8SC04228D
CC12CCC3c4ccc(O)cc4CC(CCCCCO)C3C1C=CC2=O
Reaction #277836
DOI: 10.1039/C8SC04228D
CC1(C2CCC3C4CCC5CC(O)CCC5(C)C4C(OC(=O)CCl)CC32C)OCCO1
Reaction #283072
DOI: 10.1039/C8SC04228D
Fc1ccc(C2CCC(C3CCC(CCC4OCCO4)CC3)CC2)cc1
Reaction #289081
DOI: 10.1039/C8SC04228D
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