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Regioselectivities in Diels-Alder reaction

Two proofs for the HSAB principle were provided under the restriction of a common chemical potential of the reaction partners [83, 84]. Later on, a local HSAB principle was provided by Gazqu z and Mendez [85], They showed that the interaction between two chemical species will not necessarily occur through their softest atoms, but through those whose softnesses are approximately equal. In Section 4.2, an intuitive application of the HSAB concept is provided, followed by an application of the local HSAB principle in the interpretation of regioselectivity in Diels Alder reactions. [Pg.318]

Secondary orbital interactions have also been invoked to explain regiochemistry as well as stereochemistry. Whereas 1 -substituted dienes sometimes have only a small difference between the coefficients on C-l and C-4 in the HOMO, they can have a relatively large difference between the coefficients on C-2 and C-3. Noticing this pattern, Alston suggested that the regioselectivity in Diels-Alder reactions may be better attributed, not to the primary interactions of the frontier orbitals on C-l and C-4 that we have been using so far, but to a... [Pg.235]

Table 4-2 Regioselectivity in Diels-Alder reactions predicted by considering only the frontier orbital contributions... Table 4-2 Regioselectivity in Diels-Alder reactions predicted by considering only the frontier orbital contributions...
Examination of such interactions is important for the understanding of regioselectivity in Diels-Alder reactions. Houk formulated a general approach for secondary orbital interactions. ... [Pg.940]

Interactive explanation of regioselectivity in Diels-Alder reactions... [Pg.890]

Regioselectivity in Diels-Alder reactions 889 Radicals form by homolysis of weak bonds 971... [Pg.1251]

Bansal RK, Karaghiosoff K, Gupta N, Gandhi N, Kumawata SK (2005) Diasteieo- and regioselectivity in Diels-Alder reaction of [1,4,2] diazaphospholo[4,5-a]pyridines. Tetrahedron 61 10521-10528... [Pg.233]

SCHEME 4.16 Regioselectivity in Diels—Alder reaction continued. [Pg.197]

Casetta, M. Colona, S. Manfredi, A., Hydrophobic control of organic stereochemistry. Changes of regioselectivity in Diels-Alder reactions by salt effects, Gazz. Chim. Ital, 1989, 119,533-5. [Pg.44]

Regioselectivity in Diels-Alder Reaction Regioselectivity during Diels-Alder reaction is based upon the rule that major product from Diels-Alder reaction will arise from transition state that resemble the most stable of the possible diradical intermediates that might be formed in the reaction. An... [Pg.69]


See other pages where Regioselectivities in Diels-Alder reaction is mentioned: [Pg.919]    [Pg.919]    [Pg.920]    [Pg.921]    [Pg.232]    [Pg.221]    [Pg.86]    [Pg.132]    [Pg.163]    [Pg.308]    [Pg.308]    [Pg.312]    [Pg.919]    [Pg.919]    [Pg.920]    [Pg.921]    [Pg.889]    [Pg.889]    [Pg.890]    [Pg.891]    [Pg.196]    [Pg.305]   
See also in sourсe #XX -- [ Pg.69 ]




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