Oxidative synthesis of azacyclic derivatives through the nitrenium ion: application of a hypervalent iodine species electrochemically generated from iodobenzene-Reference-Cited by-同舟云学术

Oxidative synthesis of azacyclic derivatives through the nitrenium ion: application of a hypervalent iodine species electrochemically generated from iodobenzene

Published:2006-09 Issue:37 Volume:47 Page:6505-6507
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Amano Yoshiharu,Nishiyama Shigeru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Intramolecular Cyclization with Nitrenium Ions Generated by Treatment of N-Acylaminophthalimides with Hypervalent Iodine Compounds: Formation of Lactams and Spiro-Fused Lactams

2. Synthesis of Spirodienones by Intramolecular Ipso-Cyclization of N-Methoxy-(4-halogenophenyl)amides Using [Hydroxy(tosyloxy)iodo]benzene in Trifluoroethanol

3. Synthesis of Spiro-fused Nitrogen Heterocyclic Compounds via N-Methoxy-N-acylnitrenium Ions Using Phenyliodine(III) Bis(trifluoroacetate) in Trifluoroethanol

4. Introduction of a Hydroxy Group at the Para Position and N-Iodophenylation of N-Arylamides Using Phenyliodine(III) Bis(Trifluoroacetate)

5. Novel application of N-alkoxyamides to preparative organic chemistry.

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