Copper-catalysed regioselective <i>S</i> -alkylation and C–3(H) activation of 4-hydroxydithiocoumarins and 4-hydroxy-2 <i>H</i> -chromene-2-thione: easy access to 4-methyl-3,4-dihydrothiopyran derivatives

One-pot synthesis of 4-methyl-3,4-dihydrothiopyran derivatives is accomplished from 4-hydroxydithiocoumarins/4-hydroxy-2 H -chromene-2-thione and vinyl ethers in the presence of CuI with the formation of two C–C bonds and one C–S bond.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00949a
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Copper-catalysed regioselective S -alkylation and C–3(H) activation of 4-hydroxydithiocoumarins and 4-hydroxy-2 H -chromene-2-thione: easy access to 4-methyl-3,4-dihydrothiopyran derivatives

Abu T. Khan, Prasad V. Bharatam, Santa Mondal, Mehak Sood et al.
1 citations
Organic Chemistry Frontiers
Sulfur-Based Synthesis Techniques
0.94
article

Copper-catalysed regioselective S -alkylation and C–3(H) activation of 4-hydroxydithiocoumarins and 4-hydroxy-2 H -chromene-2-thione: easy access to 4-methyl-3,4-dihydrothiopyran derivatives

Abu T. Khan, Prasad V. Bharatam, Santa Mondal, Mehak Sood, Ahmad Ali
article en
1 citations

Abstract

One-pot synthesis of 4-methyl-3,4-dihydrothiopyran derivatives is accomplished from 4-hydroxydithiocoumarins/4-hydroxy-2 H -chromene-2-thione and vinyl ethers in the presence of CuI with the formation of two C–C bonds and one C–S bond.

Organic Chemistry FrontiersVol. 12(22)
Indian Institute of Technology Guwahati (IN), National Institute of Pharmaceutical Education and Research (IN), National Institute of Pharmaceutical Education and Research (IN)
Openalex Percentile: Top 23%
Sulfur-Based Synthesis Techniques
0.94
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