Fortschritte der Chemie organischer Naturstoffe = Progress in the Chemistry of Organic Natural Products Vol. 93

Lignans, by convention, are a group of natural products that are formed by linking two phenylpropanoid units (C C units) by oxidative coupling. Most importantly, in 6 3 a lignan, two (C C units) are bound through the central carbon of their side chains, 6 3 0 i. e. the 8 and 8 positions (1, 2). The...

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Autores principales: Sahai, Mahendra, Gössinger, Edda (Autor), Luzhetska, Marta (Autor), Härle, Johannes (Autor), Begum, Sajeli A. (Autor), Ray, Anil B. (Autor)
Otros Autores: Kinghorn, Alan Douglas, 1947-...., pharmacien (Director de publicación), Falk, Heinz (Director de publicación), Kobayashi, Junichi (Director de publicación)
Formato: Livre numérique
Lenguaje:Anglais
Publicado: Vienna : Springer Vienna 2010.
Cham : Springer Nature
Colección:Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products 93
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Edition sous un autre format:• Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, Vol. 93, Texte imprimé, 9783709101391
• Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, Vol. 93, Texte imprimé, 9783709101483
• Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, Vol. 93, Texte imprimé, 9783709111079
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100 1 |a Sahai, Mahendra. 
245 1 0 |a Fortschritte der Chemie organischer Naturstoffe =  |b Progress in the Chemistry of Organic Natural Products  |n Vol. 93   |c by Mahendra Sahai, Edda Gössinger, Marta Luzhetska, Johannes Härle, Sajeli A. Begum, Anil B. Ray ; edited by A. Douglas Kinghorn, Heinz Falk, Junichi Kobayashi. 
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490 0 |a Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products  |v 93 
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520 |a Lignans, by convention, are a group of natural products that are formed by linking two phenylpropanoid units (C C units) by oxidative coupling. Most importantly, in 6 3 a lignan, two (C C units) are bound through the central carbon of their side chains, 6 3 0 i. e. the 8 and 8 positions (1, 2). The occurrence of C C -dimers, linked at sites other 6 3 0 than the 8 8 positions, is also known and these compounds have been termed neolignans (3, 4). As these two groups of compounds have close structural as well as biosynthetic relationships, they are often associated together and incorporated under the general term lignan (5). The diverse structural categorization of true lignans and of a few neolignans is presented in Fig. 1. Through the years, several review articles or books covering different facets of lignans, including their ch- istry (6, 7), biogenesis (8), synthesis (9), and biological activities (10) have been published. Enduring research for the investigation of secondary metabolites of plants has evidenced some compounds that are biogenetically related to true lignans or neolignans but bear some features not discerned in conventional lignans. These compounds or groups of compounds have been termed as non-conventional lignans , and include coumarinolignans, ?avonolignans, and stilbenolignans. The non-conventional lignans, like the conventional ones, have two C C units linked 6 3 together but have additional structural features to place them also under the category of coumarins, ?avonoids, or stilbenes. 
700 1 |a Gössinger, Edda.  |4 aut 
700 1 |a Luzhetska, Marta.  |4 aut 
700 1 |a Härle, Johannes.  |4 aut 
700 1 |a Begum, Sajeli A.  |4 aut 
700 1 |a Ray, Anil B.  |4 aut 
700 1 |a Kinghorn, Alan Douglas,  |d 1947-....,  |c pharmacien.  |4 pbd 
700 1 |a Falk, Heinz.  |4 pbd 
700 1 |a Kobayashi, Junichi.  |4 pbd 
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