Journal ArticleDOI
Chemosystematics of the lauraceae
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TLDR
Although there is a great paucity of data, the variation in the arylpropanoids, alkaloids, flavanoids and terpene constituents is in general in agreement with the subdivision of the Lauraceae.About:
This article is published in Phytochemistry.The article was published on 1972-05-01. It has received 174 citations till now.read more
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The phytochemistry of the annonaceae
TL;DR: Both alkaloidal and non-alkaloidal compounds so farsolated from Annonaceous plants are reviewed and 319 secondary products have been reported from 150 spe.
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Diversity in lignan biosynthesis
TL;DR: In this review, the phylogenetic distribution of plants producing 66 typical lignans is listed and the distribution is correlated with the putative biosynthetic pathways of the lignan and discussed from evolutionary aspects.
Journal ArticleDOI
Biosynthesis of lignans and norlignans
Shiro Suzuki,Toshiaki Umezawa +1 more
TL;DR: In this article, the authors outline the recent advances in the study of lignan and norlignan biosynthesis and present a model for biomimetic chemistry and its application.
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An historical perspective on lignan biosynthesis: Monolignol, allylphenol and hydroxycinnamic acid coupling and downstream metabolism
TL;DR: This entire 8-8′ pathway thus overall affords secoisolariciresinol and mataires inol, viewed as cancer preventative agent precursors, as well as intermediates to cancer treating substances, such as podophyllotoxin derivatives.
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Alkaloids of the rutaceae: their distribution and systematic significance☆
TL;DR: It is shown that, from the alkaloid data available, Engler's classification of the major sub-families Rutoideae and Toddalioideae is untenable and an hypothesis for the phylogeny of the Rutales, based on the distribution of alkaloids and other secondary metabolites, is proposed.
References
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Journal ArticleDOI
The phenolic constituents of plants and their taxonomic significance. I. Dicotyledons
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Studies in relation to Biosynthesis. I. Some possible routes to derivatives of Orcinol and Phloroglucinol
AJ Birch,FW Donovan +1 more
TL;DR: In this article, the head-to-tail linkage of the acetate units of a natural product containing orcinol or phloroglucinol nuclei was investigated.
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(+)-(5S)-δ-Lactone of 5-hydroxy-7-phenylhepta-2,6-dienoic acid, a natural product from Cryptocarya caloneura (Scheff.) Kostermans
JR Hlubucek,AV Robertson +1 more
TL;DR: The structure, including absolute configuration, of a new compound extracted from Cryptocarya caloneura (Scheff.) Kostermans has been determined by degradation as the (+)-(5S)-δ-lactone of 5-hydroxy-7- phenylhepta-2,6-dienoic acid.