Siloxydienes hetero Diels Alder reaction

Danishefsky and co-workers pioneered the use of chiral lanthanide complexes as catalysts in organic reactions. They found out that Eu(hfc)3, which is used as an NMR shift reagent, promoted hetero Diels-Alder reactions [30] of aldehydes with siloxydienes and induced enantiomeric enrichment (Sch. 1) [31]. Suitable substituents on the dienes were introduced to improve the extent of asymmetric induction. The best result was obtained in the reaction of benzaldehyde with l-methoxy-2-methyl-3-(trimethyl-siloxy)- , 3-butadiene using 1 mol % Eu(hfc)3 the enantiomerie excess was, however, moderate (58%). The authors maintained that the major advantage of lanthanide catalysis lay in the survival of otherwise labile systems used as adducts. 

Hetero-Diels Alder Reaction of Aldimines with Siloxydienes... 

Since Danishefsky demonstrated that activated dienes, such as siloxydiene (commonly referred to as Danishefsky s diene) react with a wide spectrum of aldehydes to afford 5,6-dihydro-y-pyrones in 1982 [l],the hetero-Diels-Alder reaction has attracted a great deal of attention over the last two decades [2,3]. The use of asymmetric catalysis in these reactions is overwhelmingly associated with heterodienophiles. Especially, the cyclocondensations of activated dienes with aldehydes or their derivatives are of particular importance, providing a multitude of opportunities for the highly efficient regio- and stereoselective construe-... 

The cycloadditions of aldehydes with chiral siloxydienes, bearing the chiral substituent at the 1-position, proceed with moderate selectivities in the presence of Eu(fod)3 or Eu(hfc)3 at low temperature. Asymmetric thermal hetero Diels-Alder reaction of triketones with 2-methyl-l-(l-phenylalkoxy)-1,3-butadienes bearing the chiral alcohols 16 or 17 (Chapter 6) as auxiliaries lead highly selective to the cycloadducts. ... 

Danishefsky and coworkers pioneered the use of chiral lanthanide complexes as catalysts in organic reactions. They found out that Eu(hfc)3, which is known as a NMR shift reagent, promoted hetero Diels-Alder reactions of aldehydes with siloxydienes and induced enantiomeric enrichment (Scheme 13.19). The best result was obtained... 

The enantioselective hetero-Diels-Alder reaction of siloxydienes, such as Danishefsky s and Brassard s dienes, with imines provides an efficient route for the preparation of functionalized nitrogen-containing heterocycles in optically active forms. Akiyama and coworkers reported the first catalytic enantioselective hetero-Diels-Alder reaction of Danishefsky s diene (21) with aromatic imines 20 using chiral phosphoric acid catalyst la (Scheme 11.7a) [14]. The desired dihydropyridi-nones 22 were obtained in good yields with high enantioselectivities. Notably, the addition of an equimolar amount of acetic acid was effective in improving the enantioselectivity. Akiyama and coworkers also reported an enantioselective... 

The enantioselective hetero Diels Alder (D A) reaction of siloxydienes, such as... 

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