Teilstruktursuche

327546

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
Ausbeute 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
Ausbeute 31.5%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #71582
steroids
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
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O[Si](c4ccccc4)(c4ccccc4)C(C)(C)C)C(OC)C3)C(C)C=CC1=O)C(C)CC2OC
Reaction #83381
17-allyl-12-[2-(4-tert-butyl-diphenylsilyloxy-3-methoxycyclohexyl)-1-methylvinyl]-1-hydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacosa-14,18-diene-2,3,10,16-tetraone
Ausbeute 72.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CCCc1ccccc1)[C@H](O)CC[C@H]1CC(F)(F)C(=O)N1CCCc1ccc(C(=O)O)s1
Reaction #87987
title compound
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C=C[C@]4(O)C[C@@H](O)CC[C@]34C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93691
3β,5-dihydroxy-15β,16β-methylene-5β-androst-6-en-17-one
Ausbeute 94.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C=C[C@]4(O)C[C@@H](O)CC[C@]34C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93694
3β,5-dihydroxy-15β,16β-methylene-5β-androst-6-en-17-one
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3C(O[SiH](C)C)CCCC3C(=O)OC(C(C)=CC3CCC(O)(C(C(C)=O)c4ccccc4)C(OC)C3)C(C)C(C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #175097
DOI: 10.1039/C8SC04228D
CC(C=O)C1CCC2C3C(OC(=O)N(C)C)C=C4CC(O)C5OC5C4(C)C3CCC12C
Reaction #193114
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)C5OCC(C)(C)CO5)C4(C)CCC3C2(C)C2OC12
Reaction #201225
DOI: 10.1039/C8SC04228D
CCOC(C)OC1(C)CCC(O[Si](CC)(CC)CC)CC(=O)OC(C(C)=CC=CC(C)CC2OC2C(C)C(CC)OC(=O)c2ccccc2)C(C)C=CC1O
Reaction #204819
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)C5OCC(C)(C)CO5)C4(C)CCC3C2(C)C2OC12
Reaction #208184
DOI: 10.1039/C8SC04228D
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3(O[SiH](c4ccccc4)c4ccccc4)CCC(C(C)(C)C)C(OC)C3)C(C)C=CC1=O)C(C)CC2OC
Reaction #210008
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(C)CC2OC)C(O)C(=O)N2CCCCC2C(=O)OC(C(C)=CC2CCC(c3ccc4ccccc4c3)C(OC)C2)C(C)C(O)CC1=O
Reaction #211644
DOI: 10.1039/C8SC04228D
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3(O[SiH](C)C)CCC(C(C)(C)C)C(OC)C3)C(C)C(OC(C)=O)CC1=O)C(C)CC2OC
Reaction #229483
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(NC(=O)COC(C)=O)C(Oc4ccccc4)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #239876
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)C5OCC(C)(C)CO5)C4(C)CCC3C2(C)C2OC12
Reaction #259453
DOI: 10.1039/C8SC04228D
Seite 1Weiter