01282nas a2200241 4500008004100000022001400041245017400055210006900229260000800298300001400306490000700320520040900327653002100736653002600757653002000783653001400803653001500817653002100832100001800853700002200871700001900893856012800912 2025 eng d a0936-521400aTetrahydrofuran ring construction through tandem iodocyclizations: synthesis of hagen's gland lactones, a pheromone of idea leuconoe , an oxylipid, and related compounds0 aTetrahydrofuran ring construction through tandem iodocyclization cSEP a2299-23030 v363 a

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.

10aCross-metathesis10aHagen's gland lactone10aIodocyclization10aoxylipids10apheromones10atetrahydrofurans1 aNookaraju, U.1 aDanve, Shivam, S.1 aKumar, Pradeep uhttps://library.ncl.res.in/content/tetrahydrofuran-ring-construction-through-tandem-iodocyclizations-synthesis-hagens-gland