Stereoselective synthesis of substituted 2,5-diazabicyclo[2.2.1]heptanes by iodine-mediated cyclization of optically pure compounds containing the 4,5-diamino-1,7-octadiene and 1,2-diamino-4-alkene moieties-Reference-Cited by-同舟云学术

Stereoselective synthesis of substituted 2,5-diazabicyclo[2.2.1]heptanes by iodine-mediated cyclization of optically pure compounds containing the 4,5-diamino-1,7-octadiene and 1,2-diamino-4-alkene moieties

Published:2007-12 Issue:50 Volume:63 Page:12446-12453
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Alvaro Giuseppe,Di Fabio Romano,Gualandi Andrea,Fiorelli Claudio,Monari Magda,Savoia Diego,Zoli Luca

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Iodine-Mediated Cyclization of (4R,5R)-4,5-Diamino-N,N′-bis[(1S)-1-phenylethyl]-1,7-octadiene - A Stereoselective Route to 2,5-Diazabicyclo[2.2.1]heptanes

2. Bicyclic Bases. Synthesis of 2,5-Diazabicyclo[2.2.1]heptanes1

3. Antifilarial agents. Diazabicyclooctanes and diazabicycloheptanes as bridged analogs of diethylcarbamazine

4. Synthesis of (1R,4R)- and (1S,4S)-2,5-Diazabicyclo[2.2.1]heptanes and TheirN-Substituted Derivatives

5. Fluoronaphthyridines and quinolones as antibacterial agents. 2. Synthesis and structure-activity relationships of new 1-tert-butyl 7-substituted derivatives

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1. Seven-membered heterocycles;Iodine-Assisted Synthesis of Six- and Seven-Membered Heterocycles;2023

2. Crystal structure of (1S,4S)-2,5-diazoniabicyclo[2.2.1]heptane dibromide;Acta Crystallographica Section E Crystallographic Communications;2017-11-17

3. Synthesis of Chiral Azabicycles from Pyroglutaminols;Organic Letters;2016-10-27

4. Octa-1,7-diene-4,5-diamine Derivatives: Useful Intermediates for the Stereoselective Synthesis of Nitrogen Heterocycles and Ligands for Asymmetric Catalysis;European Journal of Organic Chemistry;2016-06-14

5. Synthesis of (1R,4R)-2,5-diazabicyclo[2.2.1]heptane derivatives by an epimerization–lactamization cascade reaction;RSC Advances;2015