Cho, YS Kim, HY Cha, JH Pae, AN Koh, HY Choi, JH Chang, MH 2024-01-21T10:33:10Z 2024-01-21T10:33:10Z 2021-09-01 2002-06-13 1523-7060 https://pubs.kist.re.kr/handle/201004/139437 [GRAPHIC] Intramolecular Prins-type reactions of compounds having both functionalities of homoallyl alcohol and acetal moiety are described. The intramolecular Prins cyclizations were performed using indium trichloride in chloroform or 25% aqueous THE Both 9-oxabicyclo[3.3.1]nonane and 3,9-dioxabicyclo[3.3.1]nonane compounds were successfully obtained in moderate yields. English AMER CHEMICAL SOC ACETALS Indium trichloride mediated intramolecular Prins-type cyclization Article 10.1021/ol025856i 1 ORGANIC LETTERS, v.4, no.12, pp.2025 - 2028 ORGANIC LETTERS 4 12 2025 2028 scie scopus 000176185300012 2-s2.0-0013154464 Chemistry, Organic Chemistry Article ACETALS intramolecular prins-type cyclization