Aqueous Diels-Alder methodology toward some selected monoterpenes
DOI:
https://doi.org/10.26534/kimika.v18i1.1-4Keywords:
monoterpenes, aqueous Diels-Alder reaction, cycloadditionAbstract
As part of our project involving the development of synthetic protocols utilizing aqueous reaction conditions, some naturally occurring terpenes have been synthesized in our laboratory. Limonene, a-terpineol, and terpinolene were indirectly prepared via aqueous Diels-Alder reaction. The Diels-Alder reactions were carried out in water alone as medium without Lewis acid catalysis to afford the intermediates that are subsequently transformed to the target compounds by conventional means.Downloads
How to Cite
Arco, S. D., Miranda, J. T., Leaño, Jr., J. L., & Villanueva, M. U. (2002). Aqueous Diels-Alder methodology toward some selected monoterpenes. KIMIKA, 18(1), 1–4. https://doi.org/10.26534/kimika.v18i1.1-4
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