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Total synthesis of 5-desoxyleukotriene D. A new and useful equivalent of the 4-formyl-trans, trans-1,3-butadienyl anion

✍ Scribed by E.J. Corey; Dennis J. Hoover


Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
292 KB
Volume
23
Category
Article
ISSN
0040-4039

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✦ Synopsis


The first total synthesis of 5-desoxyleukotriene D (g) is reported. The route of synthesis utilizes a novel method for five-carbon chain extension. The availability of 1,4 allowed experimental demonstration that the 5-hydroxyl function is important for biological activity of the slow reacting substances.

The slow reacting substances, leukotrienes C, D, and E, are of considerable interest as a new family of highly active biological regulators which also can serve as mediators of pathological states such


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