Abstract:
To prepare ketoeicosanoids with hydropyrane fragments, new synthons were obtained from the BF3·OEt2 catalysed reaction of tri-O-acetyl-d-glucal with methyl 5-trimethylsilyloxyhex-5-enoate, methyl 10-trimethylsilyloxyundec-10-enoate and the bis(trimethylsilyl)ether of o-hydroxyacetophenone.
Document Type:
Article
Language: English
Citation:
A. G. Tolstikov, E. E. Savateeva, N. V. Khakhalina, L. V. Spirikhin, V. R. Sultanmuratova, G. A. Tolstikov, “A Short Route to Chiral Synthons: Preparation of Ketoeicosanoids with Hydropyrane Fragments”, Mendeleev Commun., 3:1 (1993), 18–20
Linking options:
https://www.mathnet.ru/eng/mendc5245
https://www.mathnet.ru/eng/mendc/v3/i1/p18
This publication is cited in the following 1 articles:
A. G. TOLSTIKOV, E. E. SAVATEEVA, N. V. KHAKHALINA, L. V. SPIRIKHIN, V. R. SULTANMURATOVA, G. A. TOLSTIKOV, “ChemInform Abstract: A Short Route to Chiral Synthons: Preparation of Keto Eicosanoids with Hydropyran Fragments.”, ChemInform, 25:33 (1994)