The biosynthetic origin of oxygen functions in phenylphenalenones of Anigozanthos preissii inferred from NMR- and HRMS-based isotopologue analysis

Author:

Munde Tobias,Maddula Ravi K.,Svatoš Aleš,Schneider Bernd

Publisher

Elsevier BV

Subject

Horticulture,Plant Science,Molecular Biology,General Medicine,Biochemistry

Reference31 articles.

1. Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro analogues by three different strategies;Baranovsky;Synth. Commun.,2003

2. Synthesis of lachanthocarpone [9-phenyl-2,6-dihydroxyphenalen-1(6)-one] by intramolecular Diels-Alder cyclization of a 1,7-diarylheptanoid orthoquinone; possible biosynthetic significance of Diels-Alder reactions;Bazan;Tetrahedron,1978

3. A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis;Brand;Planta,2006

4. Colouring matters of Australian plants. XVIII. Constituents of Anigozanthos rufus;Cooke;Aust. J. Chem.,1975

5. Naturally occurring phenalenones and related compounds;Cooke;Prog. Chem. Org. Nat. Prod.,1980

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