Explore the words cloud of the ANaPSyS project. It provides you a very rough idea of what is the project "ANaPSyS" about.
The following table provides information about the project.
Coordinator |
UNIVERSITAT KONSTANZ
Organization address contact info |
Coordinator Country | Germany [DE] |
Project website | https://www.chemie.uni-konstanz.de/gaich/ |
Total cost | 1˙497˙000 € |
EC max contribution | 1˙497˙000 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2015-STG |
Funding Scheme | ERC-STG |
Starting year | 2016 |
Duration (year-month-day) | from 2016-04-01 to 2021-03-31 |
Take a look of project's partnership.
# | ||||
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1 | UNIVERSITAT KONSTANZ | DE (KONSTANZ) | coordinator | 1˙497˙000.00 |
'Traditionally, natural products are classified into 'natural product families'. Within a family all congeners display specific structure elements, owing to their common biosynthetic pathway. This suggests a bio-inspired or 'collective synthesis', as has been devised by D: W. MacMillan. However, a biosynthetic pathway is confined to these structure elements, thus limiting synthesis with regard to structure diversification. In this research proposal the applicant exemplarily devises a strategic concept to overcome these limitations, by replacing the dogma of 'retrosynthetic analysis' with 'structure pattern recognition'. This concept is termed 'Artificial Natural Product Systems Synthesis — ANaPSyS', and aims to supersede the current 'logic of chemical synthesis' as a standard practice in this field. ANaPSyS exclusively categorizes natural products based on structural relationships — regardless of biogenetic origin. The structure pattern analysis groups natural products according to their shared core structure, and thereof creates a common precursor called 'privileged intermediate (PI)'. This intermediate is resembled in each of these natural products and is architecturally less complex. As a result every member of this natural product group can originate from a different natural product family and is obtained via this 'privileged intermediate', which serves as basis for the artificial synthetic network. With ANaPSyS a synthetic route is not restricted to a single target structure anymore (as in conventional synthesis). In comparison with bio-inspired synthesis, which is limited to a single natural product family, ANaPSyS enables the synthesis of a whole set of natural product families. With every synthesis accomplished, the network is upgraded — hence diversification leads to a rise in revenue. As a consequence, synthetic efficiency is drastically enhanced, therefore profoundly boosting and facilitating lead structure development. '
year | authors and title | journal | last update |
---|---|---|---|
2016 |
Sebastian Krüger, Tanja Gaich Total Syntheses of Vellosimine, N -Methylvellosimine, and 10-Methoxyvellosimine and Formal Synthesis of 16-Epinormacusine B through a [5+2] Cycloaddition published pages: 4893-4899, ISSN: 1434-193X, DOI: 10.1002/ejoc.201600870 |
European Journal of Organic Chemistry 2016/28 | 2019-06-19 |
2019 |
Tanja Gaich, Christa Karoline Gisela Gerlinger Structure Pattern Based Total Synthesis published pages: , ISSN: 0947-6539, DOI: 10.1002/chem.201901308 |
Chemistry – A European Journal | 2019-08-05 |
2018 |
Tanja Gaich, Heiko Rebmann, Christa K. G. Gerlinger Gramâ€scale Total Syntheses of Sarpagine Alkaloids and nonâ€Natural Derivatives published pages: , ISSN: 0947-6539, DOI: 10.1002/chem.201805644 |
Chemistry – A European Journal | 2019-08-05 |
2018 |
Christa K. G. Gerlinger, Sebastian Krüger, Tanja Gaich Total Synthesis of Parvineostemonine by Structure Pattern Recognition: A Unified Approach to Stemona and Sarpagine Alkaloids published pages: 3994-3997, ISSN: 0947-6539, DOI: 10.1002/chem.201800365 |
Chemistry - A European Journal 24/16 | 2019-05-09 |
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The information about "ANAPSYS" are provided by the European Opendata Portal: CORDIS opendata.