Three-Component Stereoselective Synthesis of (1R,2S)-1-Aryl-2-{[prop-2-yn(en)yloxy]methyl}spiro[2,4]hepta-4,7-diones
- Authors: Talybov G.M.1
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Affiliations:
- Mamedaliev Institute of Petrochemical Processes
- Issue: Vol 54, No 8 (2018)
- Pages: 1256-1259
- Section: Short Communications
- URL: https://journals.rcsi.science/1070-4280/article/view/218781
- DOI: https://doi.org/10.1134/S1070428018080225
- ID: 218781
Cite item
Abstract
Three-component reaction involving cyclopentane-1,3-dione, substituted benzaldehydes, and chloromethyl propyn(en)yl ethers results in a stereoselective formation of trans-1-aryl-2-{[prop-2-(yn)enyloxy]-methyl}spiro[2,4]hepta-4,7-diones in satisfactory yields.
About the authors
G. M. Talybov
Mamedaliev Institute of Petrochemical Processes
Author for correspondence.
Email: ahmed_adna@rambler.ru
Russian Federation, pr. Khodzhaly 30, Baku, AZ 1025 Azerbaidzhan
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