Stereoselective Synthesis of 2,6- <i>trans</i> -Tetrahydropyrans via Tandem Horner–Wadsworth–Emmons Olefination of Lactols/Intramolecular Oxa-Conjugate Cyclization
- DOI
- 10.1021/acs.joc.6c01212
- Published
- 2026-07-29
- Container
- The Journal of Organic Chemistry
- Publisher
- American Chemical Society (ACS)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/acs.joc.6c01212,
title = {Stereoselective
Synthesis of 2,6-
<i>trans</i>
-Tetrahydropyrans via Tandem
Horner–Wadsworth–Emmons
Olefination of Lactols/Intramolecular Oxa-Conjugate Cyclization},
author = {Katsiaryna A. Nekrasava and Vitaly Syakhovich and Uladzimir S. Masiuk},
year = {2026},
journal = {The Journal of Organic Chemistry},
doi = {10.1021/acs.joc.6c01212},
url = {https://doi.org/10.1021/acs.joc.6c01212}
}RIS
TY - JOUR
TI - Stereoselective
Synthesis of 2,6-
<i>trans</i>
-Tetrahydropyrans via Tandem
Horner–Wadsworth–Emmons
Olefination of Lactols/Intramolecular Oxa-Conjugate Cyclization
AU - Katsiaryna A. Nekrasava
AU - Vitaly Syakhovich
AU - Uladzimir S. Masiuk
PY - 2026
JO - The Journal of Organic Chemistry
DO - 10.1021/acs.joc.6c01212
UR - https://doi.org/10.1021/acs.joc.6c01212
ER - APA
Nekrasava, K. A., Syakhovich, V., & Masiuk, U. S. (2026). Stereoselective Synthesis of 2,6- <i>trans</i> -Tetrahydropyrans via Tandem Horner–Wadsworth–Emmons Olefination of Lactols/Intramolecular Oxa-Conjugate Cyclization. The Journal of Organic Chemistry. https://doi.org/10.1021/acs.joc.6c01212
Source records
- crossref · retrieved 2026-09-25T14:37:10.844Z