Copyright © 2025 Authors retain the copyright of this article. This article is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

@article{168376,
        author = {vinod kumar and Nitesh kumar and Rajesh kumar},
        title = {RECENT STUDIES OF STEREOSELECTIVE SYNTHESIS OF DIHYDROPYRAN TETRAHYDROPYRAN-4-ONES USING VINYL COMPOUND VIA PRINS CYCLIZATION},
        journal = {International Journal of Innovative Research in Technology},
        year = {2024},
        volume = {11},
        number = {5},
        pages = {830-836},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=168376},
        abstract = {The tetrahydropyrans (THPs), dihydropyrans (DHPs) and tetrahydropyran-4-ones (THPOs) are ubiquitous in nature. They form part structures of many important bioactive cyclic ether natural products.1 For example, substituted THPs form core structure of centrolobine (1), civet cat (2), leucascandrolide A (9), where as DHP is core structure aspergillide C},
        keywords = {Prins type cyclization reaction, tetrahydropyranic unit, vinyl sulfide, pyranone, oxonium ion},
        month = {October},
        }