Czesc,
Znalazlem m. in i te publikacje. Znalazlem rowniez i
mechanizmy tych reakcji. Osobna sprawa ile mi to
zajelo czasu.
Jurek
- Michal Sobkowski <msob_at_ibch.poznan.pl> wrote:
> At 15:21 04.03.02, Jerzy Peszke wrote:
> >Poszukuje informacji o reakcjach Dielsa-Aldera:
> retro
> >i domino.
>
> Z Beilsteina po jednym trafieniu na "Domino/Retro
> Diels-Alder reactions":
>
> Authors: Sander, Michael; Dehmlow, Eckehard
> Volker
> Journal Title: Eur.J.Org.Chem.
> Number: 2
> Publication Year: 2001
> Page: 399 - 404
> Title: Synthesis of a Substituted
> Bi[cyclohepta-3,5(3',5')-dienyl]: A
> Possible Building Block for Domino Diels-Alder
> Reactions
> Abstract: A versatile 13-step synthesis of
>
1,1'-dimethoxy-4,4'5,5'-tetrakis(trimethylsilyloxy)bicyclohepta-3,3'5,5'-dienyl
>
> (11) is described. 11 represents a potential
> building block for the
> construction of polycyclic cage compounds through
> domino Diels-Alder and
> pincer reactions.
> Keywords: Domino Diels-Alder reactions; Pincer
> reactions; Substituted
> 1,1'-dihydroxybi(cycloheptadienyl)/McMurry reactions
>
>
> Authors: Klaerner, Frank-Gerrit; Breitkopf,
> Volker
> Journal Title: Eur.J.Org.Chem.
> Number: 11
> Publication Year: 1999
> Page: 2757 - 2762
> Title: The Effect of Pressure on Retro Diels-Alder
> Reactions
> Abstract: The activation and reaction volumes
> ($DV(excit.)/$DV) were
> determined for the retro Diels-Alder reactions of
> the parent
> dihydrobarrelene 1a, its 2-cyano derivative 1b, the
> exo and endo
> Diels-Alder adducts of maleic anhydride to
> naphthalene exo-, endo-4, and
> the exo and endo Diels-Alder adducts of
> N-phenylmaleic imide to
> 6,6-dimethylfulvene exo-, endo-8 from the pressure
> dependence of the rate
> constants and the partial molar volumes (V) of
> reactants and products at
> various temperatures. The cleavage of exo-4, endo-4,
> and exo-8 are slightly
> accelerated by pressure showing negative volumes of
> activation
> ($DV(excit.)<0) whereas the others are slightly
> retarded ($DV(excit.)>0).
> From the analysis of the volume data including the
> van der Waals volumes
> (V&W%) one can conclude that the packing
> coefficients of the pericyclic
> transition states are equal to or even larger than
> those of the
> corresponding Diels-Alder adducts. This finding may
> be explained with the
> restriction of the degrees of freedom in the
> transition states leading to a
> contraction of the expansion volume.
> Keywords: High-pressure chemistry; Activation
> volumes; Reaction
> volumes; Packing coefficients; Retro Diels-Alder
> reactions
>
> Pozdrawiam,
> Michał
>
> --
> dr Michał Sobkowski
> Instytut Chemii Bioorganicznej PAN,
> Poznań
>
> http://www.man.poznan.pl/private/users/msob.html
>
>
>
>
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: Thu 08 May 2003 - 14:50:54 MET DST