A versatile route to conjugated hydroxy (E,Z,E,E)-tetraenoic acids: Highly chemo- and stereoselective synthesis of lipoxin B4

DOI: 10.1016/S0957-4166(97)00333-9

Source and publish data:

Tetrahedron Asymmetry p. 2949 - 2958 (1997)

Update date:2022-08-05

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Authors:

Alami, Mouad

Crousse, Benoit

Linstrumelle, Gerard

Mambu, Lengo

Larcheveque, Marc

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Article abstract of DOI:10.1016/S0957-4166(97)00333-9

A highly convergent total stereocontrolled synthesis of lipoxin B₄ is described by an efficient Pd-catalyzed coupling reaction of two easily accessible chiral synthons 2 and 3 without any protection-deprotection sequence of the alcohol function

Full text of DOI:10.1016/S0957-4166(97)00333-9

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