Indium trichloride mediated intramolecular Prins-type cyclization
- Authors
- Cho, YS; Kim, HY; Cha, JH; Pae, AN; Koh, HY; Choi, JH; Chang, MH
- Issue Date
- 2002-06-13
- Publisher
- AMER CHEMICAL SOC
- Citation
- ORGANIC LETTERS, v.4, no.12, pp.2025 - 2028
- Abstract
- [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.
- Keywords
- ACETALS; ACETALS; intramolecular prins-type cyclization
- ISSN
- 1523-7060
- URI
- https://pubs.kist.re.kr/handle/201004/139437
- DOI
- 10.1021/ol025856i
- Appears in Collections:
- KIST Article > 2002
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.