Teilstruktursuche

CC(C)(N)CN

CC(C)(C(N)c1ccccc1)N1CCCCC1
Reaction #49067
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(N)c1ccccc1)N1CC2CC2C1
Reaction #49075
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO[Si](C)(C)C(C)(C)C)C1(C(NC(=O)c2cccc(C(F)(F)F)c2Cl)c2ccccc2)CCCC1
Reaction #49088
title compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1(C(N)c2ccccc2)CCCCC1
Reaction #49100
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO)C1(C(NC(=O)c2cccc(C(F)(F)F)c2Cl)c2ccccc2)CCCC1
Reaction #49121
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)CCN(C2CCCCC2)C1
Reaction #53528
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@]1(C(=O)OC(C)(C)C)CCCCN1
Reaction #59637
expected product
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC1(CS(=O)(=O)N2CCC(Oc3ccc(Cl)cn3)CC2)NC(=O)NC1=O.O=C(O)C(F)(F)F
Reaction #60659
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCCCC1(CS(=O)(=O)N2CCC(Oc3ccc(Cl)cn3)CC2)NC(=O)NC1=O
Reaction #60660
N-{3-{4-[({4-[(5-chloropyridin-2-yl)oxy]piperidin-1-yl}sulfonyl}methyl]-2,5-dioxoimidazolidin-4-yl}propyl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Nc2ccc(N)cc2NC1=O
Reaction #65140
6-amino-1,2-dihydro-2,2-dimethyl-3-(4H)-quinoxalinone
DOI: 10.6084/m9.figshare.5104873.v1
Br.CC1(C)Nc2ccc(N)c(Br)c2NC1=O
Reaction #65141
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCNCC2(C)C)cc1
Reaction #71416
title compound
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #71427
title compound
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1
NCC1(N2CCN(C3CC3)CC2)CCN(Cc2ccccc2)CC1
Reaction #74273
desired product
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2CN1CC1(N2CCN(C3CC3)CC2)CCN(Cc2ccccc2)CC1
Reaction #74277
crude product
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #86027
title compound
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86028
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #86032
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86033
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1(CN)CCC2(CC1)OCCO2
Reaction #95965
8-(dimethylamino)-1,4-dioxaspiro[4.5]decane-8-methanamine
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter