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Carbonyl compound synthesis

Reaction of telluronium salts/n-BuLi with carbonyl compounds synthesis of alcohols with telluronium salt (a2) (typical procedure) A solution of n-BuLi (1.1 mmol) in hexane is added to a solution of the telluronium salt (0.459 g, 1.2 mmol) in THF (6 mL) at -78°C under N2. The mixture is warmed at -60°C and stirred for 10 min. After cooling again at -78°C, p-chlorobenzaldehyde (0.140 g, 1.0 mmol) in THF (2 mL) is added. The mixture is then allowed to warm at room temperature. After the reaction is complete (monitored by TLC), the usual work-up and flash chromatography yield pure p-chlorophenyl(phenyl)carbinol. [Pg.226]

Condensation of Enolates with Carbonyl Compounds Synthesis of Michael Acceptors... [Pg.565]

F. A. J. Meskens, Methods for the preparation of acetals from alcohols or oxiranes and carbonyl compounds, Synthesis 1981, 501. [Pg.303]

Bonnet MC, de Laat J, Dore M (1989) Etude des sous produits d ozonation de la ligmne et de glucides en milieu aqueux Environ Technol Lett 10 577-590 Chan TH, Brook MA, Chaly T (1983) A simple procedure for the acetalization of carbonyl compounds Synthesis 203 - 205... [Pg.405]

Thomas, A. D., Josemin, K. N. N., Asokan, C. V. Viismeier-Haack reactions of carbonyl compounds synthesis of substituted pyrones and pyridines. Tetrahedron 2004, 60, 5069-5076. [Pg.700]

Heterocyclic carbonyl compounds, synthesis of 81WCH231 79S633. [Pg.286]


See other pages where Carbonyl compound synthesis is mentioned: [Pg.136]    [Pg.110]    [Pg.131]   
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See also in sourсe #XX -- [ Pg.119 ]

See also in sourсe #XX -- [ Pg.119 ]

See also in sourсe #XX -- [ Pg.161 ]

See also in sourсe #XX -- [ Pg.3 ]

See also in sourсe #XX -- [ Pg.119 ]




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