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Mini-Reviews
in Organic Chemistry
ISSN: 1570-193X
Mini-Reviews
in Organic Chemistry
Volume 2, Number 1, January 2005
Contents

Utilisation of Dendritic Architectures in Molecular
Recognition and Self-Assembly Processes Pp.1-22
C.R. Yates and W. Hayes
[Abstract] [Full
text article]
Chemical and Enzymatic Synthesis of Lanthionines
Pp.23-37
M. Paul and W.A. van der Donk
[Abstract] [Full
text article]
The Enantioselective Synthesis of Conformationally
Constrained Cyclic β-Amino Acids Pp.39-45
Jason A. Miller and SonBinh T. Nguyen
[Abstract] [Full
text article]
Theoretical Studies on Domino Cycloaddition Reactions
Pp.47-57
Luis R. Domingo
[Abstract] [Full
text article]
C-Alkoxycarbonyl Nitrones: Building Blocks
for the Synthesis of Butenolides, Lactams and Modified Nucleosides
Pp.59-77
G. Romeo, D. Iannazzo, A. Piperno, R. Romeo, A. Corsaro,
A. Rescifina and U. Chiacchio
[Abstract] [Full
text article]
The Electrogenerated Cyanomethyl Anion in Organic
Synthesis Pp.79-90
L. Rossi, M. Feroci and A. Inesi
[Abstract] [Full
text article]
Recent Synthesis and Transformation of Vinylphosphonates
Pp.91-109
Valery M. Dembitsky, Abed Al Aziz Al Quntar, Abdullah
Haj-Yehia and Morris Srebnik
[Abstract] [Full
text article]
Abstracts
[Back to top]
Utilisation of Dendritic Architectures in Molecular Recognition
and Self-Assembly Processes
C.R. Yates and W. Hayes
[Full
text article]
This mini-review outlines recent key developments in the
use of dendritic architectures in selfassembly processes via
utilisation of molecular recognition motifs.
[Back to top]
Chemical and Enzymatic Synthesis of Lanthionines
M. Paul and W.A. van der Donk
[Full text
article]
Lantibiotics are peptide-derived antimicrobial agents that
are ribosomally synthesized and posttranslationally modified
to their biologically active forms. The post-translational
modifications involve the formation of dehydroalanine and
dehydrobutyrine residues and the subsequent attack of cysteines
within the peptide onto the dehydro amino acids. This generates
the so-called lanthionine and methyllanthionine thioethers
that have given lantibiotics their name. One family member,
nisin, has attracted much attention recently due to its novel
mechanism of action including specific binding to the bacterial
cell wall precursor lipid II, followed by membrane permeabilization.
Nisin has been commercially used as a food preservative, while
other lantibiotics show promising activity against bacterial
infections. This mini-review focuses on the recent developments
in the characterization of these enzymes as well as the progress
in chemical synthesis of lanthionine containing peptides.
[Back to top]
The Enantioselective Synthesis of Conformationally Constrained
Cyclic β-Amino Acids
Jason A. Miller and SonBinh T. Nguyen
[Full text
article]
Enantiomerically pure and conformationally constrained cyclic
β-amino
acids have been the subject of a vast amount of research across
the chemical, biological, and medicinal disciplines. These
valuable molecules are synthetic precursors for a wide variety
of useful compounds that include natural products and modified
peptides. Many methods have been developed to prepare chiral
cyclic β-amino
acids in high optical purity. This mini-review will discuss
some of the most recent and successful approaches.
[Back to top]
Theoretical Studies on Domino Cycloaddition Reactions
Luis R. Domingo
[Full text
article]
In this review some theoretical studies devoted to the mechanism
of domino cycloaddition reactions are summarised. The analysis
of the stationary points along the reaction pathways: transitions
structures, intermediates and adducts, allows rationalising
the chemoselectivity, regioselectivity and stereoselectivity
experimentally observed.
[Back to top]
C-Alkoxycarbonyl Nitrones: Building Blocks for the
Synthesis of Butenolides, Lactams and Modified Nucleosides
G. Romeo, D. Iannazzo, A. Piperno, R. Romeo,
A. Corsaro, A. Rescifina and U. Chiacchio
[Full
text article]
Elaboration of isoxazolidines derived from the 1,3-dipolar
cycloaddition of C-alkoxycarbonyl nitrones to suitably
substituted alkenes leads to the development of new synthetic
methodologies for the preparation of a wide range of natural
products and derivatives including lactones, lactams and complex
nucleosides. The insertion of a chiral centre in position
α,
with respect to nitrone functionality, or the presence of
a chiral auxiliary at the nitrogen atom have allowed the enantioselective
synthesis of the same compounds.
[Back to top]
The Electrogenerated Cyanomethyl Anion in Organic
Synthesis
L. Rossi, M. Feroci and A. Inesi
[Full
text article]
Suitable electrochemical methodologies for the generation
of cyanomethyl anion and some electrochemically induced cyanomethylation
reactions of electrophilic substrates are described and discussed.
In addition, the electrochemical syntheses of carbamates and
chiral oxazolidin-2-ones (under mild conditions and avoiding
the use of hazardous chemicals), via a new carboxylating
reagent (CH2CN–/CO2),
are reported in this article.
[Back to top]
Recent Synthesis and Transformation of Vinylphosphonates
Valery M. Dembitsky, Abed Al Aziz Al Quntar,
Abdullah Haj-Yehia and Morris Srebnik
[Full text
article]
Vinylphosphonates are an important group of compounds. This
review summarizes recent developments in the synthesis and
transformations of vinylphosphonates. Owing to the importance
of vinylphosphonates, many different synthetic methods have
been developed. Especially useful are various organometallic
synthetic methods utilizing the chemistry of copper, titanium,
zirconium, and lithium, etc. The transformations of vinylphosphonates
is also described and include expoxidation, cycloaddition,
Suzuki coupling, and Diels-Alder reactions.
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