Literature DB >> 32643378

Selective [3 + 2] Cycloaddition of Cyclopropenone Derivatives and Elemental Chalcogens.

Jian Wu1, Wen-Xia Gao1, Xiao-Bo Huang1, Yun-Bing Zhou1, Miao-Chang Liu1, Hua-Yue Wu1.   

Abstract

A highly efficient method is disclosed for the synthesis of 1,2-dichalcogen heterocycles via [3 + 2] cycloaddition of cyclopropenone derivatives and elemental chalcogens. Different from other cyclopropenone derivatives, cyclopropenselenones undergo unprecedented rearrangement with elemental sulfur. The features of this protocol include mild reaction conditions, high efficiency, excellent atom economy, gram-scale ability, and good regioselectivity.

Entities:  

Year:  2020        PMID: 32643378     DOI: 10.1021/acs.orglett.0c01914

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

Review 1.  Heterocycles from cyclopropenones.

Authors:  Ashraf A Aly; Alaa A Hassan; Sara M Mostafa; Asmaa H Mohamed; Esraa M Osman; AbdElAziz A Nayl
Journal:  RSC Adv       Date:  2022-06-24       Impact factor: 4.036

2.  The Fluoride Anion-Catalyzed Sulfurization of Thioketones with Elemental Sulfur Leading to Sulfur-Rich Heterocycles: First Sulfurization of Thiochalcones.

Authors:  Grzegorz Mlostoń; Jakub Wręczycki; Katarzyna Urbaniak; Dariusz M Bieliński; Heinz Heimgartner
Journal:  Molecules       Date:  2021-02-05       Impact factor: 4.411

3.  Phosphine-Catalyzed Dearomative [3 + 2] Cycloaddition of Benzoxazoles with a Cyclopropenone.

Authors:  Xingben Wang; Congjun Yu; Iuliana L Atodiresei; Frederic W Patureau
Journal:  Org Lett       Date:  2022-01-27       Impact factor: 6.005

  3 in total

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