Shin, C Chavre, SN Pae, AN Cha, JH Koh, HY Chang, MH Choi, JH Cho, YS 2024-01-21T04:38:12Z 2024-01-21T04:38:12Z 2021-09-03 2005-07-21 1523-7060 https://pubs.kist.re.kr/handle/201004/136283 A novel synthetic methodology for 2,5-disubstituted tetrahydrofurans having an allenyl group at the 3-position via Prins-type cyclization was developed. The reaction led to excellent selectivity and moderate to high yields. English AMER CHEMICAL SOC DIASTEREOSELECTIVE SYNTHESIS TRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS STEREOSELECTIVE-SYNTHESIS MEDIATED CYCLIZATIONS CONVENIENT SYNTHESIS TETRAHYDROPYRANS ETHERS CARBINOLS EPOXIDES ALCOHOLS Highly stereloselective synthesis of 2,5-disubstituted 3-vinylidene tetetrahydrofurans via Prins-type cyclization Article 10.1021/ol051058r 1 ORGANIC LETTERS, v.7, no.15, pp.3283 - 3285 ORGANIC LETTERS 7 15 3283 3285 scie scopus 000230567200038 2-s2.0-23044510870 Chemistry, Organic Chemistry Article DIASTEREOSELECTIVE SYNTHESIS TRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS STEREOSELECTIVE-SYNTHESIS MEDIATED CYCLIZATIONS CONVENIENT SYNTHESIS TETRAHYDROPYRANS ETHERS CARBINOLS EPOXIDES ALCOHOLS stereoselective tetrahydrofuran prins type cyclization