Teilstruktursuche

OC1CCNCC1

CN1CCC(Oc2ccc(C#N)cc2C(F)(F)F)CC1
Reaction #42042
objective compound
Ausbeute 64.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1CN(Cc2ccccc2)CC[C@@H]1O
Reaction #43616
desired compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(C)(O)CC1)c1ccccc1
Reaction #46638
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN([C@@H](C(=O)O)c2ccccc2)CC1
Reaction #46639
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2cnc3c(NCc4nnc5ccc(-c6cc(F)cc(F)c6)nn45)ccnc3c2)CCNCC1
Reaction #68675
4-(8-((6-(3,5-difluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylamino)-1,5-naphthyridin-3-yl)piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(O)(c2ccc(Br)cc2)CC1
Reaction #69981
4-(4-bromophenyl)-1-(methanesulphonyl)piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1(O)CCN(Cc2ccccc2)CC1
Reaction #75591
1-benzyl-4-hydroxy-4-piperidine carboxamide
Ausbeute 68.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(NC(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78239
titled compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@H](OC2CCN(C(C)=O)CC2)CC[C@@H]1C(=O)OC(C)(C)C
Reaction #89777
1-tert-butyl 2-methyl(1S,2S,4R)-4-[(1-acetylpiperidin-4-yl)oxy]cyclohexane-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCC(O)(c2ccccc2)CC1)C(F)(F)F
Reaction #94247
1-trifluoroacetyl-4-hydroxy-4-phenylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(C)(O)CC1)c1ccccc1
Reaction #155444
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN([C@@H](C(=O)O)c2ccccc2)CC1
Reaction #155445
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.CC1(C)CNCC2(CCN(C(=O)C(F)(F)F)CC2)O1
Reaction #160053
1-(10,10-dimethyl-11-oxa-3,8-diazaspiro[5.5]undecan-3-yl)-2,2,2-trifluoro-ethanone acetic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)NCC1(O)CCN(Cc2ccccc2)CC1
Reaction #166409
compound 398
Ausbeute 78.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COC2(CCN(Cc3ccccc3)CC2)CN1
Reaction #166410
compound 399
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COC2(CCNCC2)CN1
Reaction #166411
compound 400
Ausbeute 138.9%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CCC3(CC2)CNCCO3)cc1
Reaction #166413
compound 402
Ausbeute 82.7%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CCN([C@H](C)c2ccccc2)[C@H](C)C1
Reaction #167930
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC(O)CN1CCC(Oc2ccc(Cl)c(Cl)c2)CC1)c1cnc(Cl)cc1C(F)(F)F
Reaction #173054
DOI: 10.1039/C8SC04228D
COC(=O)C(C)(C)NC(=O)c1ccccc1OCC(O)CN1CCC(Oc2ccc(F)c(F)c2)CC1
Reaction #174631
DOI: 10.1039/C8SC04228D
Seite 1Weiter