Base-Promoted Cascade Double Heteroannulation of 2-Hydroxychalcones with Elemental Sulfur: An Approach to 2-Aryl-9λ <sup>4</sup> -benzo[ <i>d</i> ][1,2]oxathiolo[2,3- <i>b</i> ][1,2]oxathioles

][1,2]oxathioles via a base-promoted cascade reaction of 2-hydroxychalcones and elemental sulfur under simple heating conditions. This innovative one-pot process provides a straightforward synthetic platform for the concomitant formation of one C═S bond, two S-O bonds, and two fused heterocyclic rings with excellent atom and step efficiency. Simple, inexpensive, and readily available starting materials, operational simplicity, acceptable functional group tolerance, scalability, synthetically useful yields, and attractive product structures are some other highlighted features of this transformation. Dedicated to Prof. Habib Firouzabadi on the occasion of his 83th birthday.

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Publication Details

Journal
Organic Letters
Published
2026-06-09
DOI
https://doi.org/10.1021/acs.orglett.6c01925
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Base-Promoted Cascade Double Heteroannulation of 2-Hydroxychalcones with Elemental Sulfur: An Approach to 2-Aryl-9λ 4 -benzo[ d ][1,2]oxathiolo[2,3- b ][1,2]oxathioles

Petra Galer, Morteza Shiri, Behnaz Farajpour, Faiq H. S. Hussain et al.
Organic Letters
Sulfur-Based Synthesis Techniques
article

Base-Promoted Cascade Double Heteroannulation of 2-Hydroxychalcones with Elemental Sulfur: An Approach to 2-Aryl-9λ 4 -benzo[ d ][1,2]oxathiolo[2,3- b ][1,2]oxathioles

Petra Galer, Morteza Shiri, Behnaz Farajpour, Faiq H. S. Hussain, Azizollah Habibi, Behrouz Notash, Nafiseh Bakhshi Davoudi
article en

Abstract

][1,2]oxathioles via a base-promoted cascade reaction of 2-hydroxychalcones and elemental sulfur under simple heating conditions. This innovative one-pot process provides a straightforward synthetic platform for the concomitant formation of one C═S bond, two S-O bonds, and two fused heterocyclic rings with excellent atom and step efficiency. Simple, inexpensive, and readily available starting materials, operational simplicity, acceptable functional group tolerance, scalability, synthetically useful yields, and attractive product structures are some other highlighted features of this transformation. Dedicated to Prof. Habib Firouzabadi on the occasion of his 83th birthday.

Organic Letters
Kharazmi University (IR), Green Chemistry (PL), Sultan Qaboos University (OM), Shahid Beheshti University (IR), Alzahra University (IR), Analysis Group (United States) (US), Tishk International University (IQ)
Kharazmi University, Alzahra University
Openalex Percentile: Top 12%
Sulfur-Based Synthesis Techniques
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Base-Promoted Cascade Double Heteroannulation of 2-Hydroxychalcones with Elemental Sulfur: An Approach to 2-Aryl-9λ <sup>4</sup> -benzo[ <i>d</i> ][1,2]oxathiolo[2,3- <i>b</i> ][1,2]oxathioles — Petra Galer, Morteza Shiri, et al. · Organic Letters (2026) | TGRS Research Map | TGRS