ReviewChemical communications (Cambridge, England)2011
De novo synthesis of natural products via the asymmetric hydration of polyenes.
Review in Chemical communications (Cambridge, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed.
- Exploring a De Novo Route to Bradyrhizose: Synthesis and Isomeric Equilibrium of Bradyrhizose DiastereomersChemistry (Weinheim an der Bergstrasse, Germany) · 2024Article
- Total and Formal Syntheses of Fostriecin.Organic chemistry frontiers : an international journal of organic chemistry · 2020Article
- Cryptocaryols A and B: total syntheses, stereochemical revision, structure elucidation, and structure-activity relationship.Journal of the American Chemical Society · 2013Article
- Convergent synthesis of deoxypropionates.Angewandte Chemie (International ed. in English) · 2012Article
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Authors and funding
4 authors.
Funding
Abstract
For the last ten years our group has been working toward the development of an asymmetric hydration approach to polyketide natural products based on the regioselective hydration of di- and tri-enoates. Key to the success of this approach is the recognition that both high regiocontrol and asymmetric induction could be obtained by the use of a Sharpless asymmetric dihydroxylation reaction. Herein we describe the development of the method and its application to natural product total synthesis.
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Registered trials
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