ReviewMolecules (Basel, Switzerland)2008
Asymmetric synthesis of naturally occurring spiroketals.
Review in Molecules (Basel, Switzerland), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Benzochromanone and Benzochromene Natural Products: Synthetic Strategies and Total Syntheses.Chemical record (New York, N.Y.) · 2026Review
- Green Synthesis of Spiro Compounds with Potential Anticancer Activity through Knoevenagel/Michael/Cyclization Multicomponent Domino Reactions Organocatalyzed by Ionic Liquid and Microwave-Assisted.Molecules (Basel, Switzerland) · 2022Article
- Lewis Base Catalyzed, Sulfenium Ion Initiated Enantioselective, Spiroketalization Cascade.The Journal of organic chemistry · 2021Article
- Dictating Thermodynamic Control through Tethering: Applications to Stereoselective Bis-Spiroketal Synthesis.Angewandte Chemie (International ed. in English) · 2020Article
- ReOrganic letters · 2019Article
- Spiroacetal formation through telescoped cycloaddition and carbon-hydrogen bond functionalization: total synthesis of bistramide A.Angewandte Chemie (International ed. in English) · 2014Article
- Asymmetric synthesis of highly functionalized tetrahydropyrans via a one-pot organocatalytic Michael/Henry/ketalization sequence.Organic letters · 2014Article
- On the proposed structures and stereocontrolled synthesis of the cephalosporolides.Beilstein journal of organic chemistry · 2012Article
- Gold-catalyzed cyclizations of alkynol-based compounds: synthesis of natural products and derivatives.Molecules (Basel, Switzerland) · 2011Review
- A gold-catalyzed alkyne-diol cycloisomerization for the synthesis of oxygenated 5,5-spiroketals.Beilstein journal of organic chemistry · 2011Article
- Polyketide assembly by alkene-alkyne reductive cross-coupling: spiroketals through the union of homoallylic alcohols.Journal of the American Chemical Society · 2010Article
- Olefin metathesis-iodoetherification-dehydroiodination strategy for spiroketal subunits of polyether antibiotics.The Journal of organic chemistry · 2009Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Spiroketals are widely found as substructures of many naturally occurring compounds from diverse sources including plants, animals as well as microbes. Naturally occurring spiroketals are biologically active and most of them are chiral molecules. This article aims at reviewing the asymmetric synthesis of biologically active spiroketals for last 10 years (1998-2007).
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.