A New Biomimetic-Like Aromatization of the Cyclic End Groups of Terpenoids with Stereospecific Migration of One of the Methyl Groups: A Convenient Route to Isorenieratene (φ,φ-Carotene)-Reference-Cited by-同舟云学术

A New Biomimetic-Like Aromatization of the Cyclic End Groups of Terpenoids with Stereospecific Migration of One of the Methyl Groups: A Convenient Route to Isorenieratene (φ,φ-Carotene)

Published:2007-02 Issue:4 Volume:2007 Page:711-715
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Valla Alain,Andriamialisoa Zo,Valla Benoist,Labia Roger,Le Guillou Régis,Dufossé Laurent,Cartier Dominique

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference28 articles.

1. New Synthesis of Natural Carotene Isorenieratene (φ,φ-Carotene) and its 3,3′-Dimethoxy Analogue

2. Functional analysis of genes from Streptomyces griseus involved in the synthesis of isorenieratene, a carotenoid with aromatic end groups, revealed a novel type of carotenoid desaturase

3. A carotenogenic gene cluster from Brevibacterium linens with novel lycopene cyclase genes involved in the synthesis of aromatic carotenoids

4. Structural and functional analysis of the gene cluster encoding carotenoid biosynthesis inMycobacterium aurumA+

5. Structural and functional analysis of the gene cluster encoding carotenoid biosynthesis inMycobacterium aurumA+

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