Abstract
Chiral non-racemic perazamacrocyles containing three or more nitrogen atoms in the form of different functions (amine, amide, imine) are prepared from optically active amines, diamines, α-aminoacids, and their derivatives, by properly selected methodologies. The many applications of these optically pure perazamacrocycles rely on the basic and/or hydrogen bond donor properties of the nitrogen functions and include metal ions coordination, supramolecular chemistry, material science, molecular and enantioselective recognition, and asymmetric catalysis.
Keywords: Amines, asymmetric catalysis, chiral perazamacrocycles, cyclization, enantioselective recognition, metal complexes, porphyrins, supramolecular chemistry
Current Organic Synthesis
Title: Chiral Perazamacrocycles: Synthesis and Applications. Part 1
Volume: 6 Issue: 2
Author(s): D. Savoia and A. Gualandi
Affiliation:
Keywords: Amines, asymmetric catalysis, chiral perazamacrocycles, cyclization, enantioselective recognition, metal complexes, porphyrins, supramolecular chemistry
Abstract: Chiral non-racemic perazamacrocyles containing three or more nitrogen atoms in the form of different functions (amine, amide, imine) are prepared from optically active amines, diamines, α-aminoacids, and their derivatives, by properly selected methodologies. The many applications of these optically pure perazamacrocycles rely on the basic and/or hydrogen bond donor properties of the nitrogen functions and include metal ions coordination, supramolecular chemistry, material science, molecular and enantioselective recognition, and asymmetric catalysis.
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Cite this article as:
Savoia D. and Gualandi A., Chiral Perazamacrocycles: Synthesis and Applications. Part 1, Current Organic Synthesis 2009; 6 (2) . https://dx.doi.org/10.2174/157017909788167301
DOI https://dx.doi.org/10.2174/157017909788167301 |
Print ISSN 1570-1794 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6271 |
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