بحث البنية الفرعية

CCCCC(C)CCCCCBr

C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)C(=O)CC[C@@H]12
Reaction #50340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53928
trans-4-(5-Bromo-pentyl)-cyclohexylamine
المردود 129.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(N[C@H]1CC[C@H](CCCCCBr)CC1)c1ccc(C(F)(F)F)cc1
Reaction #53929
trans-N-[4-(5-Bromo-pentyl)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide
المردود 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCO)CCCCC[C@H]1CC[C@H](NS(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53930
trans-N-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-4-trifluoromethyl-benzenesulfonamide
المردود 80.2%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53935
trans-[4-(5-Bromo-pentyl)-cyclohexyl]-methyl-amine hydrobromide
المردود 179.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)CCC[C@@H](C)CBr
Reaction #55056
(2R,6R)-(-)-1-bromo-2,6,10-trimethylundecane
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C#N)(CCCCCn1ccnc1)c1ccc(Cl)cc1Cl
Reaction #56546
product
المردود 47.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](N3CCOCC3)[C@@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](C(=O)CBr)CC[C@@H]12
Reaction #64870
(2β,3α,5α)-21-bromo-3-hydroxy-2-(4-morpholinyl)pregnan-20-one
DOI: 10.6084/m9.figshare.5104873.v1
C#CC12CC3CC(C#C)(C1)CC(C14CC5CC(C#C)(CC(C#C)(C5)C1)C4)(C3)C2
Reaction #67394
3,3′,5,5′-tetraethynyl-1,1′-biadamantane
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C(Br)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
Reaction #78037
4-Bromo-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C1(CCCCCBr)CCCC1
Reaction #182522
DOI: 10.1039/C8SC04228D
CC12CC(=O)C3C(CCC4CC(O)CCC43C)C1CCC2C(=O)CSCc1ccccc1
Reaction #188340
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
BrCCCCCC1CCCCC1
Reaction #200378
DOI: 10.1039/C8SC04228D
CC1CCC2(OC1)OC1CC3C4CCC5CC(=O)C=CC5(C)C4CCC3(C)C1C2C
Reaction #200852
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(CCBr)CC1
Reaction #203072
DOI: 10.1039/C8SC04228D
C=CC12CCc3cc(O)ccc3C1C(CCCCCN1CCCCC1)CC1(C)C(O)CCC12
Reaction #203881
DOI: 10.1039/C8SC04228D
CC12CCC3C(CC=C4CCCCC43C)C1CC(Br)C2=O
Reaction #210265
DOI: 10.1039/C8SC04228D
CC12CCC(O)CC1CCC1C2CCC2(C)C(C(=O)COc3ccncc3)CCC12
Reaction #212328
DOI: 10.1039/C8SC04228D
الصفحة 1التالي