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CCC1(CC)CO1

CC(C)(C)[Si](C)(C)OC[C@@H]1CC(=O)[C@H]1CO[Si](C)(C)C(C)(C)C
Reaction #6046
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1OC12CCOCC2
Reaction #48663
desired compound
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(O)C1(F)CCOCC1
Reaction #48664
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CCC45OC4C(=O)CC[C@H]35)[C@@H]1CC/C2=C\Cl
Reaction #52574
E-17-Chloromethylene-4ξ,5ξ-epoxy-estran-3-one
DOI: 10.6084/m9.figshare.5104873.v1
C1CCCCCC2(CCCCC1)CO2
Reaction #65581
title compound
Ausbeute 78.7%DOI: 10.6084/m9.figshare.5104873.v1
O=CC1CCCCCCCCCCC1
Reaction #65582
clear oil
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2C3CCC2CC2(CO2)C3)cc1
Reaction #68978
8-Benzyl-spiro[8-azabicyclo[3.2.1]octane-3,2′-oxirane]
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CC(=O)[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O
Reaction #70380
5α-hydroxyandrostane-3,6,17-trione
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccccc2)CC23OC2C=CC=C13
Reaction #74751
colorless solid
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccc(Cl)cc2)CC23OC2C=CC=C13
Reaction #74753
2-(p-Chlorobenzylidene)-1-indanone oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccc(-c2c3c(nn2CCCN2CCOCC2)-c2ccccc2C3)cc1
Reaction #74755
cream-colored material
Ausbeute 134.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC2(CC1)CO2
Reaction #75586
benzyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate
Ausbeute 71.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(F)(CO)CC1
Reaction #75587
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(O)(CF)CC1
Reaction #75590
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(N(C)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78240
titled compound
Ausbeute 75.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](NCCCNCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92660
Dendrogenin B
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCCCNCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92661
5α-Hydroxy-6β-[4-(3-aminopropylamino)-butylamino]-cholestan-3β-ol
Ausbeute 50.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92662
5α-Hydroxy-6β-(4-aminobutylamino)-cholestan-3β-ol
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92663
5α-Hydroxy-6β-(3-aminopropylamino)-cholestan-3β-ol
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN[C@@H]1C[C@H]2[C@@H]3CC[C@H]([C@H](C)CCCC(C)C)[C@@]3(C)CC[C@@H]2[C@@]2(C)CC[C@H](O)C[C@]12O
Reaction #92664
5α-Hydroxy-6β-(3-propylamino)-cholestan-3β-ol
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
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