Di-sec-butyl ketone

Di iso-butvlamine Di-sec-butylamme Di-iso-butyl ketone Di-tert-butvl ketone... [Pg.470]

Lithium tetrahydridoaluminate di-tert-butyl ketone Sec. alcohols from ketones Stereospecific reduction... [Pg.23]

Hindered phenolates have low nucleophilicity and in aprotic solvent may act usefully as EGBs. 2,6-Di-t-butyl-/ -cresol = 16.8) was reduced directly with concomitant hydrogen evolution to give, ex situ, the corresponding tetraethylammonium phenolate [59,60], which was clearly capable of deprotonating aromatic ketones and in the presence of aromatic aldehydes promoted aldol reaction to a, /3-unsaturated ketones which underwent Michael addition. The initial proton transfer from the aromatic ketone ] K = 24.7) is thermodynamically very unfavorable. Even so, aldol reaction took place within a matter of hours upon addition of an aromatic ketone together with an aromatic aldehyde leading to or, /3-unsaturated ketones which subsequently underwent Michael addition with a sec-... [Pg.1243]

Compound Name Sec-butyl Alcohol Butylene Oxide Butylene Oxide Butylene Oxide N-Butyl Acetate Di-N-Butyl Ether Di-N-Butyl Ether Ethylhexaldehyde Ten-Butyl Hydroperoxide N-Butyl Mercaptan N-butyl Methacrylate N-Butyl Methacrylate N-Butyl Methacrylate Methyl N-Butyl Ketone N-Butyl Methacrylate P-T en-Butylphenol Dibutyl Phthalate N-Butyl Acrylate Tetrabutyl Titanate Tetrabuiyl Titanate 2,4,5-T(Esters)... [Pg.133]