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CC(C)CC(C)(C)C

CCCCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60424
1-butyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
Выход 75.7%DOI: 10.6084/m9.figshare.5104873.v1
CSCCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60443
1-(2-methylsulfanylethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
Выход 70.5%DOI: 10.6084/m9.figshare.5104873.v1
CSCCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1.Cl
Reaction #60444
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCNCC2)c(C2CC(C)(C)CC(C)(C)C2)c1
Reaction #60465
title compound
Выход 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCN(c2ccc(C)cc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60466
1-[4-methyl-2-(3,3,5,5-tetramethylcyclohexyl)phenyl]-4-propylpiperazine
Выход 89.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60477
1-allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60478
1-prop-2-ynyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC#CCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60479
1-but-2-ynyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCNCC2)c(C2CC(C)(C)CC(C)(C)C2)c1
Reaction #60493
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCN(CC3CCOCC3)CC2)c(C2CC(C)(C)CC(C)(C)C2)c1
Reaction #60494
1-[4-methoxy-2-(3,3,5,5-tetramethylcyclohexyl)phenyl] -4-(tetrahydropyran-4-ylmethyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCN(c2ccc(OC)cc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60495
1-butyl-4-[4-methoxy-2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2c(N)cccc2F)CC(C)(C)C1
Reaction #60515
title compound
Выход 31.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2c(F)cccc2N2CCNCC2)CC(C)(C)C1
Reaction #60516
title compound
Выход 26.8%DOI: 10.6084/m9.figshare.5104873.v1
N#CCOc1ccc(-c2ccc(/C=C/C(=O)O)cc2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #70006
(E)-3-(3′-Adamantan-1-yl-4′-cyanomethoxybiphenyl-4-yl)-acrylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)[C@@]1(c2ccccc2)C[C@@H]2C[C@H]1CC2Oc1cc2cc[nH]c(=O)c2cc1Cl
Reaction #73471
desired product
Выход 100.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@H](CCBr)CCCBr)(c1ccccc1)c1ccccc1
Reaction #82298
(S)-(-)-3-(tert-butyldiphenylsilyloxymethyl)-1,6-dibromohexane
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)C2CNCC21.Cl
Reaction #83683
(3aRS,7aRS)-7,7-dimethyl-4-perhydroisoindolone hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)C2CN(Cc3ccccc3)CC21
Reaction #83684
(3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindolone
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=CC(=O)C2CN(Cc3ccccc3)CC21
Reaction #83710
(3aRS,7aRS)-2-benzyl-7,7-dimethyl-2,3,3a, 4,7,7a-hexahydro-1H-4-isoindolone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@H](CCBr)CCCBr)(c1ccccc1)c1ccccc1
Reaction #83723
(S)-(-)-3-(tert-butyldiphenylsilyloxymethyl)-1,6-dibromohexane
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
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