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Non-ionic base

Verkade JG (2003) P(RNCH2CH2)3N Very Strong Non-ionic Bases Useful in Organic Synthesis. [Pg.239]

Varvoglis A (2003) Preparation of Hypervalent Iodine Compounds. 224 69-98 Verkade JG (2003) P(RNCH2CH2)3N Very Strong Non-ionic Bases Useful in Organic Synthesis. 223 1-44... [Pg.234]

Because of their non-ionic base they find application in both cationic and anionic emulsion systems. [Pg.263]

Strong and Hindered Bases in Organic Synthesis. ChemFiles 2003, 5(1). Verkade, J.G. P(RNCH2CH2)3N Very strong non-ionic bases useful in organic synthesis. Topics Curr. Chem. 2002, 223, 1-44. [Pg.270]

Schwesinger, R. (1985) Extremely strong, non-ionic bases syntheses and applications. Chimia, 39, 269-272. [Pg.7]

Kovacevic, B., Baric, D. and Maksic, Z.B. (2004) Basicity of exceedingly strong non-ionic bases in acetonitrile - Verkade s superbase and some related phosphazenes. New Journal of Chemistry, 28, 284-288. [Pg.46]

Kingston, J.V. and Verkade, J.G. (2005) P[N( Bu)CH2CH2]3N Aversatile non-ionic base for the synthesis of higher coordinate silicates. Inorganic Chemistry Communications, 8, 643-646. [Pg.47]

P(RNCH2CH2)bN Very Strong Non-Ionic Bases Useful in Organic Synthesis 3... [Pg.3]

One of the earliest strong non-ionic bases to make its appearance was Proton Sponge and its derivatives [1] and these systems have been reviewed [2]. More recently Proton Sponge has been used in the palladium-catalyzed arylation of 2,3-dihydrofuran [3], and it also catalyzes Knoevenagel condensations of substrates possessing activated methylene groups [4]. [Pg.4]


See other pages where Non-ionic base is mentioned: [Pg.1337]    [Pg.207]    [Pg.267]    [Pg.224]    [Pg.349]    [Pg.132]    [Pg.261]    [Pg.235]    [Pg.238]    [Pg.1023]    [Pg.865]    [Pg.255]    [Pg.223]    [Pg.309]    [Pg.132]    [Pg.1530]    [Pg.329]    [Pg.197]    [Pg.159]    [Pg.253]    [Pg.315]    [Pg.147]    [Pg.3]   
See also in sourсe #XX -- [ Pg.202 ]




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