73435-80-0Relevant academic research and scientific papers
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)
Valla, Alain,Andriamialisoa, Zo,Valla, Benoist,Labia, Roger,Le Guillou, Regis,Dufosse, Laurent,Cartier, Dominique
, p. 711 - 715 (2007/10/03)
The synthesis of isorenieratene, a natural carotenoid isolated from the marine sponge Reniera japonica and from some anoxygenic phototrophic bacteria or nonphotosynthetic actinomycetes, was performed from α-, β- and retro-ionones. In this series of cycloh
New Synthesis of Natural Carotene Isorenieratene (φ,φ-Carotene) and its 3,3′-Dimethoxy Analogue
Valla, Alain R.,Cartier, Dominique L.,Valla, Benoist G.,Le Guillou, Regis Y.,Andriamialisoa, Zo R.,Labia, Roger,Breithaupt, Dietmar E.,Savy, Stephanie M.,Binet, Adrien,Dufosse, Laurent H.
, p. 3314 - 3319 (2007/10/03)
The main pigments of Brevibacterium linens are the aromatic carotenoids 3,3′-dihydroxyisorenieratene (ψ,ψ-carotene-3,3′-diol), the corresponding monohydroxy compound, and the hydrocarbon isorenieratene. We report herein new syntheses of isorenieratene (φ,
