ReviewBeilstein journal of organic chemistry2016
The direct oxidative diene cyclization and related reactions in natural product synthesis.
Review in Beilstein journal of organic chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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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
3 citing papers in PubMed.
- Dual Co/Photoredox-Catalyzed Regio- and Stereoselective Allyl Homocoupling Providing Functionalized 1,5-Dienes.Organic letters · 2026Article
- Ru-catalysed oxidative cyclisation of 1,5-dienes: an unprecedented role for the co-oxidant.RSC advances · 2020Article
- Ligand Substitution of RuChemistry (Weinheim an der Bergstrasse, Germany) · 2020Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The direct oxidative cyclization of 1,5-dienes is a valuable synthetic method for the (dia)stereoselective preparation of substituted tetrahydrofurans. Closely related reactions start from 5,6-dihydroxy or 5-hydroxyalkenes to generate similar products in a mechanistically analogous manner. After a brief overview on the history of this group of transformations and a survey on mechanistic and stereochemical aspects, this review article provides a summary on applications in natural product synthesis. Moreover, current limitations and future directions in this area of chemistry are discussed.
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