Search results for "allylboration"

showing 3 items of 3 documents

Stereoselective synthesis of the published structure of synargentolide A and of one of its stereoisomers

2005

A stereoselective synthesis is described of the structure published for the naturally occurring synargentolide A, an α,β-unsaturated lactone. The key steps of the synthesis were a Brown´s asymmetric allylation and a ring closing metathesis. The spectroscopic data of the synthetic product were very close to those of the natural product but did not exactly match them. An epimer of the published structure was then synthesized according to a similar strategy. Again, the data of the synthetic product did not match those reported for the natural product. It is thus likely that the actual structure of synargentolide A differs from the published one in more than mere stereochemical aspects. Marco V…

Asymmetric allylborationUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Ring-closing metathesisUNESCO::QUÍMICA::Química orgánicaSynargentolide A:QUÍMICA [UNESCO]Synargentolide A ; Ring-closing metathesis ; Asymmetric allylboration ; Asymmetric dihydroxylationAsymmetric dihydroxylation
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Recent Developments in the Chiral Brønsted Acid-catalyzed Allylboration Reaction with Polyfunctionalized Substrates

2016

Asymmetric allylboration has played a central role in organic synthesis ever since the pioneering work by Hoffman and Brown, having found applications in the total synthesis of many natural products. A new dawn for this 40 year-old reaction occurred with the beginning of the new century when the first catalytic asymmetric methods came into play. In less than one decade, several methodologies, able to achieve the desired homoallylic alcohols with ee ranges in the high 90s, were developed. Among them, in the present account, we will disclose our contribution to the development of the chiral binolphosphoric-derived BrOnsted acid-catalyzed allylboration of aldehydes originally reported by Antil…

chemistry.chemical_classification010405 organic chemistryChemistryGeneral Chemical Engineeringasymmetric allylborationTotal synthesisGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryAldehyde0104 chemical sciencesCatalysischiral BrOnsted acid catalysischemistry.chemical_compounddensity functional calculationsMaterials ChemistryOrganic chemistryOrganic synthesisdiversity-oriented synthesisBrønsted–Lowry acid–base theoryallylic compoundsThe Chemical Record
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Recent developments and applications of the chiral Brønsted acid catalyzed allylboration of carbonyl compounds

2018

The 50-year-old allylboration reaction has seen dramatic developments since the dawn of the new century after the first catalytic asymmetric versions came into play. In the past decade alone, several methodologies capable of achieving the desired homoallylic alcohols in over 90% ee have been developed. This review focuses on the chiral Brønsted acid catalyzed allylboration reaction, covering everything from the very first examples and precedents to modern day variations and applications.1 Introduction2 Early Developments3 Synthetic Applications4 Variants5 Computational Contribution6 Conclusions

enantioselective catalysis010405 organic chemistryChemistryOrganic Chemistryasymmetric synthesisEnantioselective synthesis010402 general chemistryDFT calculations01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysishomoallylic alcoholsallylborationchiral Brønsted acidsBrønsted–Lowry acid–base theoryenantioselective catalysis­chiral BrOnsted acids
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