Участвует в 12 реакциях

3621

CCCCC[Si@H]1CC[C@H](c2cc(F)c(C[C@@H](C)CC)c(F)c2)CC1
Reaction #2744
(S)-4-(trans-4-n-pentyl-4-silacyclohexyl)-1-(2-methylbutyl)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC[Si@H]1CC[C@H]([C@H]2CC[C@H](c3ccc(C[C@@H](C)CC)cc3)CC2)CC1
Reaction #2748
(S)-4-(trans-4-(trans-4-n-pentyl-4-silacyclohexyl)cyclohexyl)-1-(2- methylbutyl) benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCOc1ccc(-c2ncc(C[C@@H](C)CC)cn2)cc1
Reaction #361385
(S)-2-(p-Heptyloxyphenyl)-5-(2-methylbutyl)-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCOC(=O)C(C[C@@H](C)CC)C(=O)OCC
Reaction #432903
diethyl (S)-2-methylbutylmalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
CC[C@H](C)COc1ccc([C@H](CO)NC(=O)OC(C)(C)C)cc1
Reaction #542154
title compound
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CC[C@H](C)COc1ccc(O)cc1
Reaction #741598
white crystals
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_07
CC[C@H](C)C[Si](C)(Cl)Cl
Reaction #814009
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CC[C@H](C)C[Si](Cl)(Cl)c1ccccc1
Reaction #814010
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CCOC(=O)c1cnn(-c2ccc(OC[C@@H](C)CC)c(C#N)c2)c1
Reaction #937258
ethyl 1-(3-cyano-4-((S)-2-methylbutoxy)phenyl)pyrazole-4-carboxylate
Выход 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
C#Cc1c(C[C@@H](C)CC)ccc2ccccc12
Reaction #1099029
1-Ethynyl-2-(2-(S)-methylbutyl)naphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CCCCCCCOc1ccc(-c2ncc(C[C@@H](C)CC)cn2)cc1
Reaction #1621586
(S)-2-(p-Heptyloxyphenyl)-5-(2-methylbutyl)-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_02
CCCCCCCOc1ccc(-c2ncc(C[C@@H](C)CC)cn2)cc1
Reaction #1850102
(S)-2-(p-Heptyloxyphenyl)-5-(2-methylbutyl)-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_05