Ostatnie postępy w syntezie alkaloidów tropanowych i pochodnych tropanu
Journal Title: Wiadomości Chemiczne - Year 2015, Vol 69, Issue 11
Abstract
Tropane alkaloids are a long-known class of compounds possessing an 8-azabicyclo[ 3.2.1]octane skeleton. Many tropane alkaloids posses biological activity (anticholinergic, anti-Parkinsonian, hypotensive), and as such had a significant influence on medicine and played a notable role in the development of organic chemistry [1]. The most known representatives of biologically active tropane alkaloids are: cocaine, atropine, scopolamine, ecgonine, and Bao Gong Teng A. A number of natural tropane alkaloids are chiral compounds, whose preparation in optically active forms is still a big challeng [2]. The biological activity of enantiomers often differs depending on their configurations. Alkaloids are a subject of an intensive research: scopus database contains nearly 200 thousand publications with the word „alkaloid”, and almost 4,500 publications with the phrase „tropane alkaloids” (about half of them have appeared in the last ten years). About 55 papers are devoted to stereoselective synthesis of tropane derivatives in 2000-2015. About half of this concernes stereoselective methods. The organic synthesis of alkaloids has a long history and numerous synthetic approaches to the tropane skeleton have been developed, from the classical synthesis of tropinone by Willstätter at the beginning of the XX century, to more recent developments dealing with asymmetric deprotonation of tropinone with chiral lithium amide bases for the enantioselective synthesis of a range of tropanes [3, 4]. Owing to extensiveness of the field, the current review presents the most interesting, from a synthetic point of view, approaches to tropane derivatives and tropane analogues. Most of the methods of synthesis are long (often several steps), time- and recourses-intensive, and often required elaborate and hardly available starting materials. But there are also notable exceptions, based on the asymmetric deprotonation approach; e.g., from the syntheses of cocaine described in this article, the most efficient one was reported by Lee in 2000 [5]. The concise synthesis (6 steps) gave the unnatural enantiomer of cocaine starting from commercially available tropinone in 78% overall yield. This approach allows to obtain both enantiomers and racemate, by changing type of one reactant only. However, most strategies provide only one enantiomer or racemic mixture of an alkaloid. As can be seen, despite of advances in chemicall science, there is no general way to synthesize majority of the representatives of this group of structurally related compounds.
Authors and Affiliations
Katarzyna Sidorowicz, Krzysztof Kropiwnicki, Ryszard Łaźny
Keywords
Related Articles
- EP ID EP585208
- DOI -
- Views 116
- Downloads 0
Biologiczna synteza nanocząstek metali
Nanotechnology has attracted a great interest in recent years due to its expected impact on many areas such as energy, medicine, electronics and space industries. One of the most important aspects in researching nanotech...
Syntezy wybranych leków pochodnych 2-amino-1H-benzimidazolu
2-Amino-1H-benzimidazole fragment occurs in broad spectrum of drugs with anticancer, antiviral, antifungal, anthelmintic and antihistamine properties. There are 30 drugs, 2-amino-1H-benzimidazole derivatives, registered...
Kultowe bestie : literatura a nauka
Wampire, werewolf or zombie are individuals more and more often met in horrors. Since their existence seems to break down all rules of science literature experts consider them exclusively as metaphor of human anxiety tow...
Białka błony zewnętrznej fusobacterium nucleatum jako potencjalny czynnik promocji nowotworu jelita grubego
Fusobacterium nucleatum is a Gram-negative, anaerobic bacterium located in an oral cavity. This bacterium can migrate with blood to the different part of the human body e.g colon. The studies suggest participation of Fn...
Wybrane właściwości fizykochemiczne polikarboksylanowych związków kompleksowych kobaltu(II), niklu(II), miedzi(II) i oksowanadu(IV
Cobalt(II), nickel(II), copper(II) and oxidovanadium(IV) cations are coordination centers in many polycarboxylate complexes [1‒16]. A number of coordination compounds of transition metal ions with such ligands as polycar...