Expanding the silyl-Prins toolbox: selective access to C4-quaternary stereocenters in tetrahydropyrans using internal cyclopropylsilyl alcohols

The use of internal cyclopropylsilyl alcohols in Prins cyclization is reported as a methodology for the stereoselective construction of tetrahydropyrans bearing a quaternary stereocenter.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00984g
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
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article

Expanding the silyl-Prins toolbox: selective access to C4-quaternary stereocenters in tetrahydropyrans using internal cyclopropylsilyl alcohols

Alberto Cherubin, Asunción Barbero, Paula González-Andrés
Organic Chemistry Frontiers
Synthetic Organic Chemistry Methods
article

Expanding the silyl-Prins toolbox: selective access to C4-quaternary stereocenters in tetrahydropyrans using internal cyclopropylsilyl alcohols

Alberto Cherubin, Asunción Barbero, Paula González-Andrés
article en

Abstract

The use of internal cyclopropylsilyl alcohols in Prins cyclization is reported as a methodology for the stereoselective construction of tetrahydropyrans bearing a quaternary stereocenter.

Organic Chemistry FrontiersVol. 12(23)
Universidad de Valladolid (ES)
Openalex Percentile: Top 84%
Synthetic Organic Chemistry Methods
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Expanding the silyl-Prins toolbox: selective access to C4-quaternary stereocenters in tetrahydropyrans using internal cyclopropylsilyl alcohols — Alberto Cherubin, Asunción Barbero, et al. · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS