Synthesis of 6- to 10-membered ring (E)-hydroxyiminohydroazaazoniabenzocycloalkenes derivative from cyclization of 2-nitromethylene-1-(ω-phenylalkyl)imidazolidine or 2-nitromethylene-1-(ω-phenylalkyl)hexahydropyrimidine in trifluoromethanesulfonic acid-Reference-Cited by-同舟云学术

Synthesis of 6- to 10-membered ring (E)-hydroxyiminohydroazaazoniabenzocycloalkenes derivative from cyclization of 2-nitromethylene-1-(ω-phenylalkyl)imidazolidine or 2-nitromethylene-1-(ω-phenylalkyl)hexahydropyrimidine in trifluoromethanesulfonic acid

Published:2006-04 Issue:14 Volume:62 Page:3320-3328
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Coustard Jean-Marie,Soro Yaya,Siaka Sorho,Bamba Fanté,Cousson Alain

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference31 articles.

1. Mild method for the synthesis of amidines by the electrophilic activation of amides

2. Structures of New Pseudo-Peptide Antibiotics, Sperabillins

3. Pyrrole-3-carbamidine: A lethal principle from Nierembergia hippomanica

4. N-Azinylpyridinium N-aminides: tandem reactions with α-halocarbonyl derivatives and analogs

5. A Potent Inhibitor of Inducible Nitric Oxide Synthase, ONO-1714, a Cyclic Amidine Derivative

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