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Alanes pyridines

The pyridine ring is easily reduced in the form of its quaternary salts to give hexahydro derivatives by catalytic hydrogenation [446], and to tetrahydro and hexahydro derivatives by reduction with alane aluminum hydride) [447], sodium aluminum hydride [448], sodium bis 2-methoxyethoxy)aluminum hydride [448], sodium borohydride [447], potassium borohydride [449], sodium in ethanol [444, 450], and formic acid [318]. Reductions with hydrides give predominantly 1,2,5,6-tetrahydro derivatives while electroreduction and reduction with formic acid give more hexahydro derivatives [451,452]. [Pg.56]

Financial support was provided by the National Science Foundation (Grant CHE-94-13128). Prof. Alan Bond and Mr. Richard Webster provided advance information concerning their studies on the electrochemistry of pyridine 2,6-dithioesters and related substances84. [Pg.637]

Donor-r acceptor (D-rA) interactions. The combination of donor and acceptor sites raises the possibility of D A interactions (intramolecular and intermolecular). In most systems, such D A interactions are prevented by the steric demand of the substituents (steric frustration) and/or the nature of the organic linker (geometric frustration). Noticeable exceptions are illustrated in Scheme 1 (i) the Cj-bridged phosphine-alane 3 adopts a head-to-tail dimeric structure and is usually reacted in the presence of an additional Lewis base to displace the A1 interactions " (ii) the di- and tri-phosphine boranes 7 and 8 equilibrate in solution between open and closed forms which were unambiguously identified in the solid state by X-ray diffraction analyses (iii) the pyridine-borane 2 exists in solution as a mixture of closed monomeric form and head-to-tail dimeric structure, but N B interactions are readily cleaved upon coordination to Ru. ... [Pg.240]

The Lansbury reagent, formed as the product of the reaction between pyridines with lithium tetrahydroaluminate (Hthium alanate), has been employed as a useful reducing agent in organic chemistry for a long time. Hensen and coworkers demonstrated that Lansbury reagent has the... [Pg.54]


See other pages where Alanes pyridines is mentioned: [Pg.45]    [Pg.290]    [Pg.371]    [Pg.384]    [Pg.487]    [Pg.335]    [Pg.1037]    [Pg.230]    [Pg.141]    [Pg.274]    [Pg.347]    [Pg.362]    [Pg.269]   
See also in sourсe #XX -- [ Pg.8 , Pg.580 ]

See also in sourсe #XX -- [ Pg.8 , Pg.580 ]




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Alanates

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Alanes

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