10581-28-9Relevant articles and documents
Synthesis of 6-tert-octyl and 6,8-ditert-butyl coumarins, two coumarins of biological interest
Arroyo, P.,Darouch, M.,Lisboa, E.,Miranda, A.,Zárraga, M.
, p. 5220 - 5222 (2021/07/12)
In this study, the synthesis of new coumarins with aliphatic chains is discussed. The incorporation of the 6-tert-octyl and 6,8-ditert-butyl chains into a coumarin structure from alkylphenols, allows obtaining hydrophobic coumarins with good yields. These coumarins can be potential modulators of TRPV1 receptors. Synthesis and spectroscopic data of these new coumarins are analyzed.
Campestarenes: Novel shape-persistent Schiff base macrocycles with 5-fold symmetry
Guieu, Samuel,Crane, Angela K.,MacLachlan, Mark J.
supporting information; experimental part, p. 1169 - 1171 (2011/03/20)
A simple 1-step procedure yields a family of easily modifiable, stable, conjugated Schiff base macrocycles with 5-fold symmetry mediated by 3-center hydrogen bonding.
Nickel complex catalyzed reduction of imines
Vetter,Berkessel
, p. 419 - 422 (2007/10/02)
The 1:1 complexes formed in situ from nickel(II) acetate and the thiosemicarbazones of ortho-hydroxy aromatic aldehydes catalyze the hydrosilylation of imines. A variety of imines were reduced in good to excellent yields employing two equivalents of a silane such as triethylsilane and 5 mol% of the catalysts.
