Recherche de Sous-structure

C1CNCCC1CCO

[N-]=[N+]=NCCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #956
4-Azidoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CC2(CCNCC2)CO1
Reaction #75621
3-oxo-2-oxa-8-azaspiro[4.5]decane hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(NC(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78239
titled compound
Rendement 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C2(CCOS(C)(=O)=O)CCN(C(c3ccccc3)(c3ccccc3)c3ccccc3)CC2)c1
Reaction #83742
4-Methanesulfonyloxyethyl-4-(3-methylphenyl)-N-tritylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(NC(=O)c2c(C)nc3c(OCC4CCCCC4)cccn23)CCNCC1
Reaction #92753
methyl[4-({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)piperidin-4-yl]acetate
Rendement 97.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@]2(CCO2)CCN1[C@H](C)c1ccccc1
Reaction #168031
(4S,6R)-6-methyl-7-((R)-1-phenylethyl)-1-oxa-7-azaspiro[3.5]nonane
Rendement 30.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCC1(N2CCCC2)CCNCC1
Reaction #177316
DOI: 10.1039/C8SC04228D
FC(F)(F)c1ccc(COCCC2CCNCC2)cc1
Reaction #177389
DOI: 10.1039/C8SC04228D
Cn1cnc2c(C#N)nc(-c3ccc(OCCC4CCN(C(=O)CCl)CC4)c(C(F)(F)F)c3)cc21
Reaction #179254
DOI: 10.1039/C8SC04228D
CCC1CC2CC(O)=C(OC)C=C2CN1Cc1cc(OC)c(OC)c(OC)c1
Reaction #184209
DOI: 10.1039/C8SC04228D
C(=C(c1ccccc1)c1ccccc1)C1CCNCC1
Reaction #190100
DOI: 10.1039/C8SC04228D
CC(C)CCC(COC(F)F)N1CCC(CC(=O)O)CC1c1ccc(C(F)(F)F)cc1
Reaction #190445
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
CC(O)CNC(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #196522
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCBr)C1CCN(Cc2ccccc2)CC1
Reaction #201133
DOI: 10.1039/C8SC04228D
Cc1cc(C)cc(C2(CCO)CCN(Cc3ccccc3)CC2)c1
Reaction #202696
DOI: 10.1039/C8SC04228D
Cl
Reaction #205728
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)C1CCN(Cc2ccccc2)CC1
Reaction #210178
DOI: 10.1039/C8SC04228D
CCN(CC)CCOCCC1CCN(C(=O)N2c3cc(Cl)ccc3C(=O)Nc3cccnc32)CC1
Reaction #210867
DOI: 10.1039/C8SC04228D
CCOC(=O)CC1CCN(C(C)=O)CC1
Reaction #214038
ethyl 1-acetyl-4-piperidineacetate
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
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