Karaarslan, MDemircan, A2019-08-012019-08-0120060970-70770975-427Xhttps://hdl.handle.net/11480/5544Synthesis towards the precursor 1 for radicalic reaction has been studied. 3-Methyl-5-(5-methylfuran-2-yl)-4,5-dihydro-isoxazole, (7) was obtained from vinyl furan. 2-(4-lodo-pent-4-enyl)-4methyl-6-(5-methyl-furan-2-yl)-[1,3]oxazinane (13) was generated using the amino alcohol 8 and corresponding aldehyde (11). Selective protection on the amino alcohol was achieved. Steric hindrance of amino group behaved obstructive to a condensation reaction.eninfo:eu-repo/semantics/closedAccesssynthesisfuranintra-intermolecularheteroradicalic cyclizationSynthesis of new furan compounds: A study towards pyrrole ringArticle1816456492-s2.0-29244453282Q4WOS:000233608100098Q4