Reverse-Cope cyclisations of thiahydroxylamines derived from the addition of allylic thiols to nitrones: Syntheses of 1,3-thiazolidine-N-oxides and 1,5,2-oxathiazinanes-Reference-Cited by-同舟云学术

Reverse-Cope cyclisations of thiahydroxylamines derived from the addition of allylic thiols to nitrones: Syntheses of 1,3-thiazolidine-N-oxides and 1,5,2-oxathiazinanes

Published:1997-12 Issue:49 Volume:38 Page:8549-8552
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Coogan Michael P,Gravestock Michael B,Knight David W,Thornton Steven R

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Factors influencing the reverse-Cope approach to 1,2,5-oxadiazinanes from allylamines and nitrones: Optimization of a new vicinal diamine synthesis

2. Retro-Cope eliminations in the synthesis of 1,2,5-oxadiazinanes from allylamines and nitrones: a method for the amination of unactivated alkenes

3. Cyclization of unsaturated hydroxylamine derivatives

4. Nitrones and oxaziridines. XXII. Preparation and cyclization of some δ,ε-unsaturated hydroxylamines

5. The regiochemistry of intramolecular n-alkenylnitrone additions: preparative and mechanistic implications

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4. ChemInform Abstract: Reverse-Cope Cyclizations of Thiahydroxylamines Derived from the Addition of Allylic Thiols to Nitrones: Syntheses of 1,3-Thiazolidine-N-oxides and 1,5,2-Oxathiazinanes.;ChemInform;2010-06-23

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