5--Trig vs 6--Trig α-acyliminium ion-olefin cyclisations stereoselective synthesis of 7-(1-formyloxy-pent-1-yl)-1-aza-4-oxa-spiro[4.5]decane-2-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. A formal synthesis of (±)-perhydrohistrionicotoxin via α-acylimmonium ion-olefin cyclizations
2. A short and stereoselective synthesis of perhydrohistrionicotoxin
3. Rules for ring closure
4. J.D. Schagen and A.R. Overbeek, to be published.
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1. Thirty-five years of synthetic studies directed towards the histrionicotoxin family of alkaloids;Natural Product Reports;2007
2. Cyclizations of N-Acyliminium Ions;Chemical Reviews;2004-03-01
3. Asymmetric synthesis of spiro 2-pyrrolidin-5-ones, 2-piperidin-6-ones and 1-isoindolin-3-ones. Part 2: N-Acyliminium ion cyclisations with an internal alkene nucleophile;Tetrahedron;2004-01
4. A biomimetic synthesis of the pyrrolizidine ring by sequential intramolecular cyclizations;Tetrahedron Letters;2000-01
5. Novel spiro cyclisations of N-acyliminium ions involving an aromatic π-nucleophile;Tetrahedron Letters;1994-09
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