Keum, GC Kang, SB Kim, Y Lee, E 2024-01-21T06:45:27Z 2024-01-21T06:45:27Z 2021-09-02 2004-06-10 1523-7060 https://pubs.kist.re.kr/handle/201004/137490 Tetrahydrofuranyl allyl carbinols may be prepared stereoselectively via radical cyclization of beta-alkoxyvinyl sulfoxides, Pummerer rearrangement, and reaction with allylstannane. English AMER CHEMICAL SOC Stereoselection in radical cyclization of beta-alkoxyvinyl sulfoxides: Synthesis of tetrahydrofuranyl allyl carbinols Article 10.1021/ol049676f 1 ORGANIC LETTERS, v.6, no.12, pp.1895 - 1897 ORGANIC LETTERS 6 12 1895 1897 scie scopus 000221868300004 2-s2.0-3042833041 Chemistry, Organic Chemistry Article tetrahydrofuranyl carbinol pummerer rearrengement allylstannane