Conformationally controlled transannular reactions of a 12-membered macrocyclic trienol

DOI: 10.1016/S0957-4166(00)80285-2

Source and publish data:

Tetrahedron Asymmetry p. 415 - 430 (1992)

Update date:2022-08-02

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Authors:

Padron Padron

Vazquez Vazquez

Morales Morales

Zarraga Zarraga

Martin Martin

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Article abstract of DOI:10.1016/S0957-4166(00)80285-2

Iodine-induced transannular ring enlargements of several epoxide derivatives of the cyclotrienol (Z,E,Z)-1-hydroxy-cyclododeca-2,5,9-triene (1) are presented. The diastereoselection exhibited by both the inter- and intramolecular reactions studied, appear

Full text of DOI:10.1016/S0957-4166(00)80285-2

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Product name:4-Bromo-benzoic acid (2Z,5E,9Z)-cyclododeca-2,5,9-trienyl ester

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