Recherche de Sous-structure

C=CCCCCCCCCCBr

C=CCCCCCCCCCBr
Reaction #9894
11-bromo-undec-1-ene
Rendement 82.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9895
(S)-3-(1-methyl-pyrrolidin-2-yl)-1-undec-10-enyl-pyridinium bromide
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCC2C3C=CC4=CC(=O)C=CC4(C)C3C(F)CC12C
Reaction #184077
DOI: 10.1039/C8SC04228D
N#CC1C=CC2=C(CCCCC2)C1=O
Reaction #186787
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)C=CC4(C)C3CCC21C
Reaction #192000
DOI: 10.1039/C8SC04228D
CC12CCC(O)C=C1CCC1C2C(=O)CC2(C)C(C(=O)CBr)CCC12
Reaction #192455
DOI: 10.1039/C8SC04228D
CC12CCC3C(CC=C4CCCCC43C)C1CC(Br)C2=O
Reaction #210265
DOI: 10.1039/C8SC04228D
C=CCCCCCCCCCN(C)C(C)=O
Reaction #217075
1-(N-methylacetamido)-10-undecene
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CC2=CC=C3C4CCC(C(C)CBr)C4(C)CCC3C2(C)C(OC(C)=O)C1
Reaction #234477
DOI: 10.1039/C8SC04228D
CC12C=CC(=O)C=C1C(Br)CC1C2CCC2(C)C(=O)CCC12
Reaction #235405
DOI: 10.1039/C8SC04228D
C=CCCCCCCCCCCCO
Reaction #244436
DOI: 10.1039/C8SC04228D
SCCCCCCCCCCCBr
Reaction #261737
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=O)C1=CCC2C3CCC4=CC(=O)CCC4(C)C3(F)C(Br)CC12C
Reaction #266612
DOI: 10.1039/C8SC04228D
CC12CCC3C(CC(Cl)C4(O)CC=CCC34C)C1CC=C2Br
Reaction #286615
DOI: 10.1039/C8SC04228D
CC1CCC2(C)C(=CCC3C4CC(O)C(=O)C4(C)CCC32)C1
Reaction #288865
DOI: 10.1039/C8SC04228D
FC(F)(Cl)C=CCCCCCCCCCOc1ccc(Cl)cc1
Reaction #294388
DOI: 10.1039/C8SC04228D
C[C@]12CC[C@H]3[C@@H]([C@@H](O)C=C4C[C@@H](O)CC[C@@]43C)[C@@H]1C[C@@H](O)[C@@H]2O
Reaction #360879
3β,7β,16α,17β-tetrahydroxyandrost-5-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(=O)C=C1CCC1C2=CCC2(C)C1CCC2(O)C(=O)CBr
Reaction #391933
DOI: 10.1039/C8SC04228D
CC1CCC2(OC1)OC1C=C3C4CCC5CC(=O)C(=N)CC5(C)C4CC(=O)C3(C)C1C2C
Reaction #395322
DOI: 10.1039/C8SC04228D
COC(=O)OC1CC2=CC=C3C4CCC(C(C)CBr)C4(C)CCC3C2(C)C(OC(=O)OC)C1
Reaction #399085
DOI: 10.1039/C8SC04228D
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