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ChemInform Abstract: A Versatile Route to Conjugated Hydroxy (E,Z,E,E)-Tetraenoic Acids: Highly Chemo- and Stereoselective Synthesis of Lipoxin B4.

✍ Scribed by M. ALAMI; B. CROUSSE; G. LINSTRUMELLE; L. MAMBU; M . LARCHEVEQUE

Publisher
John Wiley and Sons
Year
2010
Weight
41 KB
Volume
29
Category
Article
ISSN
0931-7597

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✦ Synopsis

Highly Chemo-and Stereoselective Synthesis of Lipoxin B 4 .

-Ongoing interest in the field of Pd-coupling reactions leads to the efficient synthesis of the methyl ester (XIII) of the title compound. This highly chemo-and stereoselective approach without using protection-deprotection sequences of hydroxy groups may be useful for the synthesis of other polyenic alcohols. -(ALAMI, M.;

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