Switchable Reactivity of Glycals Toward the Synthesis of 3‐Oxo Glycals and 2‐Deoxy Lactones

Abstract The switchable reactivity of glycals has been demonstrated by the successful synthesis of 3‐oxo glycals and 2‐deoxy lactones directly from glycals under ambient conditions. 3‐Oxo glycals were obtained from various glycals via C3‐oxidation employing (NH 4 ) 2 S 2 O 8 as an oxidant in DMSO solvent at 55 °C. However, 2‐deoxy lactones were synthesized through C‐1 oxidation using Pd(OAc) 2 as a catalyst and K 2 S 2 O 8 as an oxidant in the DMSO:H 2 O solvent system. The methodology is operationally simple, high‐yielding, scalable, and endowed with varied substrate scope.

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Publication Details

Journal
ChemistrySelect
Published
2025-08-25
DOI
https://doi.org/10.1002/slct.202504180
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
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article

Switchable Reactivity of Glycals Toward the Synthesis of 3‐Oxo Glycals and 2‐Deoxy Lactones

Nazar Hussain, Manish K. Sharma, Anand Kumar Pandey
ChemistrySelect
Carbohydrate Chemistry and Synthesis
article

Switchable Reactivity of Glycals Toward the Synthesis of 3‐Oxo Glycals and 2‐Deoxy Lactones

Nazar Hussain, Manish K. Sharma, Anand Kumar Pandey
article en

Abstract

Abstract The switchable reactivity of glycals has been demonstrated by the successful synthesis of 3‐oxo glycals and 2‐deoxy lactones directly from glycals under ambient conditions. 3‐Oxo glycals were obtained from various glycals via C3‐oxidation employing (NH 4 ) 2 S 2 O 8 as an oxidant in DMSO solvent at 55 °C. However, 2‐deoxy lactones were synthesized through C‐1 oxidation using Pd(OAc) 2 as a catalyst and K 2 S 2 O 8 as an oxidant in the DMSO:H 2 O solvent system. The methodology is operationally simple, high‐yielding, scalable, and endowed with varied substrate scope.

ChemistrySelectVol. 10(33)
Zero to Three (US), Institute of Medical Sciences (IN), Banaras Hindu University (IN)
Openalex Percentile: Top 83%
Carbohydrate Chemistry and Synthesis
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