Zhang, Qi and Catti, Lorenzo and Syntrivanis, Leonidas-Dimitrios and Tiefenbacher, Konrad. (2019) En route to terpene natural products utilizing supramolecular cyclase mimetics. Natural Product Reports. Epub.
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Official URL: https://edoc.unibas.ch/72303/
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Abstract
Covering: literature up to 2018Terpenes are a class of natural products characterized by remarkable structural diversity. Much of this diversity arises biosynthetically from a handful of linear precursors through the so-called tail-to-head terpene cyclization reaction. This reaction is one of the most complex observed in nature, and historically attempts to replicate it with non-enzymatic means have met with little success. In recent years, however, the development of manmade binding pockets that allow such reactions to take place has been reported. This Highlight provides an overview of this nascent field, and outlines the challenges that need to be overcome moving forward.
Faculties and Departments: | 05 Faculty of Science > Departement Chemie > Chemie > Synthesis of Functional Modules (Tiefenbacher) |
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UniBasel Contributors: | Tiefenbacher, Konrad Karl |
Item Type: | Article, refereed |
Article Subtype: | Research Article |
Publisher: | The Royal Society of Chemistry |
ISSN: | 0265-0568 |
e-ISSN: | 1460-4752 |
Note: | Publication type according to Uni Basel Research Database: Journal article |
Language: | English |
Identification Number: |
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edoc DOI: | |
Last Modified: | 23 Oct 2019 07:47 |
Deposited On: | 23 Oct 2019 07:47 |
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