Teilstruktursuche

1220734

—
Reaction #86068
oil
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C2CCCC2)n[nH]1
Reaction #86069
5-cyclopentyl-2H-pyrazol-3-ylamine
Ausbeute 46.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(C2CC3(C)C(CCC4C5CCC(C(=O)CC#N)C5(C)CC(=O)C43)CC2O)CCO1
Reaction #233199
DOI: 10.1039/C8SC04228D
CC1(C)CN([C@H]2C[C@@]3(C)[C@@H](CC[C@H]4[C@@H]5CC[C@H](C(=O)CC#N)[C@@]5(C)CC(=O)[C@@H]43)C[C@@H]2O)CCO1
Reaction #320704
(2β,3α,5α)-3-hydroxy-2-(2,2-dimethyl-4-morpholinyl)-11,20-dioxopregnane-21-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN([C@H]2C[C@@]3(C)[C@@H](CC[C@@H]4[C@@H]3CC[C@]3(C)[C@@H](C(=O)CSC#N)CC[C@@H]43)C[C@@H]2O)CCO1.CS(=O)(=O)O
Reaction #320706
(2β,3α,5α)-3-hydroxy-2-(2,2-dimethyl-4-morpholinyl)-21-thiocyanatopregnan-20-one methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
N#CCC(=O)C1CCCC1
Reaction #718617
3-cyclopentyl-3-oxopropanenitrile
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC(=O)C1CCCC1
Reaction #911111
DOI: 10.1039/C8SC04228D
N#CCC(=O)C1CCCC1
Reaction #913107
DOI: 10.1039/C8SC04228D
N#CCC(=O)C1CCCC1
Reaction #958662
3-cyclopentyl-3-oxopropanenitrile
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC(=O)C1CCCC1
Reaction #1002738
3-cyclopentyl-3-oxopropanenitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-n1nc(C2CCCC2)cc1N
Reaction #1002739
3-cyclopentyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC(=O)C1CCCC1
Reaction #1185746
3-cyclopentyl-3-oxopropanenitrile
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C2CCCC2)no1
Reaction #1185747
3-cyclopentylisoxazol-5-amine
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC(=O)C1CCCC1
Reaction #1584422
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(C2CCCC2)nc2cc(F)c(Cl)cc2c1-c1ccccc1
Reaction #1584426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(C2CCCC2)nc2ccc(C(F)(F)F)cc2c1-c1ccccc1
Reaction #1584436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(-c3ccccc3)c(C#N)c(C3CCCC3)nc2c1
Reaction #1584446
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(C2CCCC2)nc2ccc(C(F)(F)F)cc2c1O
Reaction #1584451
title compound
Ausbeute 32.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(C#N)c(C3CCCC3)nc3ccc(Cl)cc23)ccn1
Reaction #1584457
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCC(=O)C1CCCC1
Reaction #1644098
DOI: 10.1039/C8SC04228D
Seite 1Weiter