Tetrahydrofuran ring construction through tandem iodocyclizations: synthesis of hagen's gland lactones, a pheromone of idea leuconoe , an oxylipid, and related compounds

TitleTetrahydrofuran ring construction through tandem iodocyclizations: synthesis of hagen's gland lactones, a pheromone of idea leuconoe , an oxylipid, and related compounds
Publication TypeJournal Article
Year of Publication2025
AuthorsNookaraju, U, Danve, SS, Kumar, P
JournalSynlett
Volume36
Issue15
Pagination2299-2303
Date PublishedSEP
Type of ArticleArticle
ISSN0936-5214
KeywordsCross-metathesis, Hagen's gland lactone, Iodocyclization, oxylipids, pheromones, tetrahydrofurans
Abstract

A simple and efficient common route was developed for the syntheses of tetrahydrofuran-ring-containing natural products such as Hagen's gland lactones and their epimers, a pheromone of the butterfly Idea leuconoe, an oxylipid, and some valuable synthons. Brown's allylation, cross-metathesis, iodocyclization, and a tandem aminoxylation/allylation were employed as key steps in the syntheses.

DOI10.1055/a-2550-1785
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

1.4

Divison category: 
Organic Chemistry
Database: 
Web of Science (WoS)

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