A convenient synthetic route to 2-aryl-N-tosylazetidines and their ZnX2 (X=I, OTf) mediated regioselective nucleophilic ring opening reactions: synthesis of γ-iodoamines and tetrahydropyrimidines-Reference-Cited by-同舟云学术

A convenient synthetic route to 2-aryl-N-tosylazetidines and their ZnX2 (X=I, OTf) mediated regioselective nucleophilic ring opening reactions: synthesis of γ-iodoamines and tetrahydropyrimidines

Published:2006-07 Issue:30 Volume:47 Page:5393-5397
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ghorai Manas K.,Das Kalpataru,Kumar Amit,Das Animesh

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference48 articles.

1. Nucleophilic ring opening of aziridines

2. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

3. Recent Synthetic Applications of Chiral Aziridines

4. Aziridines: epoxides’ ugly cousins?

5. Synthesis and Ring Opening of Methyl 2-Alkyl-3-(alkyl/aryl)-1-benzoylaziridine-2-carboxylates: Synthesis of Polysubstituted Amino Acids

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