@article {49776,
	title = {Tetrahydrofuran ring construction through tandem iodocyclizations: synthesis of hagen{\textquoteright}s gland lactones, a pheromone of idea leuconoe , an oxylipid, and related compounds},
	journal = {Synlett},
	volume = {36},
	year = {2025},
	month = {SEP},
	pages = {2299-2303},
	type = {Article},
	abstract = {<p>
	A simple and efficient common route was developed for the syntheses of tetrahydrofuran-ring-containing natural products such as Hagen{\textquoteright}s gland lactones and their epimers, a pheromone of the butterfly Idea leuconoe, an oxylipid, and some valuable synthons. Brown{\textquoteright}s allylation, cross-metathesis, iodocyclization, and a tandem aminoxylation/allylation were employed as key steps in the syntheses.</p>
},
	keywords = {Cross-metathesis, Hagen{\textquoteright}s gland lactone, Iodocyclization, oxylipids, pheromones, tetrahydrofurans},
	issn = {0936-5214},
	doi = {10.1055/a-2550-1785},
	author = {Nookaraju, U. and Danve, Shivam S. and Kumar, Pradeep}
}
