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CC(C)C(C=C)O

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
CN(C)c1ccc(Nc2nc3cc(OC4(C5CCN(CCNC=O)C5)C=CC=CN4)ccc3n2C)cc1
Reaction #41737
4-(2-{[4-(dimethylamino)phenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nc3cc(OC4(C5CCN(CCNC=O)C5)C=CC=CN4)ccc3n2C)ccc1Br
Reaction #41739
4-(2-{[4bromo-3-methylphenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(Nc2nc3cc(OC4(C5CCN(CCNC=O)C5)C=CC=CN4)ccc3n2C)cc1
Reaction #41746
4-(2-{[4-ethylphenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC1(C3CCN(CCNC=O)C3)C=CC=CN1)nc(Nc1ccc(Cl)cc1)n2C
Reaction #41772
4-(2-{[4-chlorophenyl]amino-6-methoxy-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(N)=O)c(C)c(I)c1Br
Reaction #45571
compound
Ausbeute 50.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1C(=O)C=CC1O
Reaction #68749
5-(4′-chloro-4-ethylbiphen-3-yl)-4-hydroxy-cyclopent-2-enone
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1C(=O)C=CC1=O
Reaction #68750
2-(4′-chloro-4-ethylbiphen-3-yl)cyclopent-4-ene-1,3-dione
Ausbeute 80.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #71582
steroids
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccccc2)CCC23OC2C=CC=C13
Reaction #74750
semi-crystalline residue
Ausbeute 102.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#C/C=C/C23OC2(C)CCCC3(C)C)nc1
Reaction #81518
Ethyl (±)-6-[(3E)-4-(1,2-Epoxy-2,6,6-trimethylcyclohexanyl)but-3-en-1-ynyl)nicotinate
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#C[C@]1(O)C(=C)C[C@H]2[C@@H]3CC(=C)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@@]21C
Reaction #93683
title compound
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
CCCCC(C)(C)C(/C=C/I)OC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #95290
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C)(C)C(C=CI)OC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #174131
DOI: 10.1039/C8SC04228D
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