Shin, Chul Oh, Youna Cha, Joo Hwan Pae, Ae Nim Choo, Hyunah Cho, Yong Seo 2024-01-21T01:06:33Z 2024-01-21T01:06:33Z 2021-09-05 2007-03-05 0040-4020 https://pubs.kist.re.kr/handle/201004/134544 Prins-type cyclization followed by palladium-catalyzed cyclization provided sterically congested bi- or tricyclic tetrahydrofurans, which are very stereoselective as well. cis-2,5-Disubstituted tetrahydrofurans obtained from Prins-type cyclization have an allenyl group and a functional group such as alcohol, carboxylic acid, and aryl halide. The tetrahydrofurans bearing an allene group underwent palladium-catalyzed cyclization to give sterically congested bi- or tricyclic tetrahydrofurans. (c) 2007 Elsevier Ltd. All rights reserved. English PERGAMON-ELSEVIER SCIENCE LTD PRINS-TYPE CYCLIZATION SAKURAI ISMS REACTION DIASTEREOSELECTIVE SYNTHESIS ENANTIOSELECTIVE SYNTHESIS THERMAL BENZANNULATION TETRAHYDROPYRANS MONOCERIN CONSTRUCTION DERIVATIVES ANTIFUNGAL Synthesis of sterically congested bicyclic tetrahydrofurans via Pd-catalyzed cyclization Article 10.1016/j.tet.2006.12.080 1 TETRAHEDRON, v.63, no.10, pp.2182 - 2190 TETRAHEDRON 63 10 2182 2190 scie scopus 000244536500009 2-s2.0-33846618144 Chemistry, Organic Chemistry Article PRINS-TYPE CYCLIZATION SAKURAI ISMS REACTION DIASTEREOSELECTIVE SYNTHESIS ENANTIOSELECTIVE SYNTHESIS THERMAL BENZANNULATION TETRAHYDROPYRANS MONOCERIN CONSTRUCTION DERIVATIVES ANTIFUNGAL