Synthesis of carbocyclic and heterocyclic β-aminocarboxylic acids
In consequence of their biological effects, conformationally constrained carbocyclic β-amino
acids have generated great interest among synthetic and medicinal chemists in the past 2 …
acids have generated great interest among synthetic and medicinal chemists in the past 2 …
Hydrolases in the Stereoselective Synthesis of N-Heterocyclic Amines and Amino Acid Derivatives
E Busto, V Gotor-Fernández, V Gotor - Chemical reviews, 2011 - ACS Publications
Chiral nitrogenated compounds are highly attractive compounds because of their
importance in agrochemicals, fine chemicals, and pharmaceuticals but also due to their …
importance in agrochemicals, fine chemicals, and pharmaceuticals but also due to their …
Highly functionalized cyclic β-amino acid moieties as promising scaffolds in peptide research and drug design
Peptide-based drug research has received high attention in the field of medicinal chemistry
over the past decade. For drug design, to improve proteolytic stability, it is desirable to …
over the past decade. For drug design, to improve proteolytic stability, it is desirable to …
Lewis Acid‐Catalyzed [3+ 2] Cycloaddition of Donor‐Acceptor Cyclopropanes and Enamines: Enantioselective Synthesis of Nitrogen‐Functionalized Cyclopentane …
K Verma, P Banerjee - Advanced Synthesis & Catalysis, 2016 - Wiley Online Library
A straightforward and efficient method for the synthesis of nitrogen‐functionalized
cyclopentane derivatives via [3+ 2] cycloaddition of enamines with donor‐acceptor …
cyclopentane derivatives via [3+ 2] cycloaddition of enamines with donor‐acceptor …
A novel and selective fluoride opening of aziridines by XtalFluor-E. Synthesis of fluorinated diamino acid derivatives
The selective introduction of fluorine onto the skeleton of an aminocyclopentane or
cyclohexane carboxylate has been developed through a novel and efficient fluoride opening …
cyclohexane carboxylate has been developed through a novel and efficient fluoride opening …
[HTML][HTML] Chloramine-T (N-chloro-p-toluenesulfonamide sodium salt), a versatile reagent in organic synthesis and analytical chemistry: An up to date review
YN Nayak, SL Gaonkar, EAM Saleh… - Journal of Saudi …, 2022 - Elsevier
Abstract Chloramine-T (CAT), the sodium salt of N-chloro-p-toluenesulfonamide, is a low-
cost mild oxidizing agent with a wide range of uses. Most importantly, it can be used in …
cost mild oxidizing agent with a wide range of uses. Most importantly, it can be used in …
Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds
Fluorine‐containing organic molecules have generated increasing impact in drug research
over the past decade. Their preparation and development of novel synthetic methods …
over the past decade. Their preparation and development of novel synthetic methods …
Recent advances in the transformations of cycloalkane-fused oxiranes and aziridines
This account highlights the most relevant transformations of cycloalkane-fused oxiranes and
aziridines developed during the past decade with the intention to provide an overview of the …
aziridines developed during the past decade with the intention to provide an overview of the …
Nature's Toolbox for the Hydrolysis of Lactams and Cyclic Imides
P Stockinger, R Buller - ACS Catalysis, 2024 - ACS Publications
Hydrolytic enzymes, such as lactamases or hydantoinases, can be valuably applied to
convert lactams (cyclic amides) and cyclic imides into optically pure compounds, for …
convert lactams (cyclic amides) and cyclic imides into optically pure compounds, for …
Recent progress in the selective fluorinations of some functionalized cycloalkenes
Organofluorine compounds have had an increasing impact in synthetic organic chemistry
and pharmaceutical research over the past two decades. Their syntheses and the …
and pharmaceutical research over the past two decades. Their syntheses and the …