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Acrylic acid Chiral resolution

The Diels-Alder reaction of ester-tethered trienes is also known as a powerful methodology to construct polycylic Y lactones [68]. Romo et al. [69] surveyed effective organic nucleophilic catalysts for tandem intermolecular Diels-Alder reaction/lactonization reaction of achiral a, 3-unsaturated acid chlorides with dienyl alcohol 100 (Scheme 45). In this case, when chiral Lewis base 102 was used as a nucleophilic catalyst, excellent enantioselectivity was realized. Lipase-catalyzed domino kinetic resolution/intramolecular Diels-Alder reaction of furfuryl alcohols with acrylic acids was also carried out by Akai and Kita [70]. [Pg.274]

See other pages where Acrylic acid Chiral resolution is mentioned: [Pg.814]    [Pg.334]    [Pg.336]    [Pg.257]    [Pg.316]    [Pg.1352]    [Pg.15]    [Pg.150]    [Pg.73]    [Pg.23]    [Pg.14]    [Pg.133]    [Pg.29]    [Pg.145]    [Pg.532]    [Pg.166]    [Pg.170]    [Pg.352]    [Pg.284]    [Pg.155]    [Pg.98]   
See also in sourсe #XX -- [ Pg.1411 ]



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Acrylic acid Chirality

Chiral acids

Chiral acrylates

Chiral resolution

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