scholarly journals Recent advances in the synthesis of α-amino ketones

Author(s):  
Lewis A. T. Allen ◽  
Robert-Cristian Raclea ◽  
Philipp Natho ◽  
Philip J. Parsons

This review on α-amino ketone synthesis collates and evaluates developments made in this area over the past decade, with an extended discussion on functional group compatibility, resultant product substitution patterns, and medicinal applications.

Molecules ◽  
2020 ◽  
Vol 25 (21) ◽  
pp. 4906
Author(s):  
Jurriën W. Collet ◽  
Thomas R. Roose ◽  
Bram Weijers ◽  
Bert U. W. Maes ◽  
Eelco Ruijter ◽  
...  

Isocyanides have long been known as versatile chemical reagents in organic synthesis. Their ambivalent nature also allows them to function as a CO-substitute in palladium-catalyzed cross couplings. Over the past decades, isocyanides have emerged as practical and versatile C1 building blocks, whose inherent N-substitution allows for the rapid incorporation of nitrogeneous fragments in a wide variety of products. Recent developments in palladium catalyzed isocyanide insertion reactions have significantly expanded the scope and applicability of these imidoylative cross-couplings. This review highlights the advances made in this field over the past eight years.


1970 ◽  
Vol 43 (1) ◽  
pp. 156-170 ◽  
Author(s):  
A. Eisenberg ◽  
M. Shen

Abstract Since the publication of our review “Glass Transition in Polymers” in 1966, a number of interesting advances have been made in this field. The present article is intended to be an addendum to this review, reporting the progress that has been made by various workers during the past three years. In addition, a number of topics were not covered in the previous article due to the relatively incomplete understanding at that time. These will now be discussed. This is not because these topics are at present fully understood. Rather, we hope it will serve as a progress report to stimulate further interest in areas where further work is needed. The numbering systems and notations in this paper will follow those in the previous article for the sake of continuity.


2021 ◽  
Vol 17 ◽  
pp. 2462-2476
Author(s):  
Yi Liu ◽  
Puying Luo ◽  
Yang Fu ◽  
Tianxin Hao ◽  
Xuan Liu ◽  
...  

Great progress has been made in the tandem annulation of enynes in the past few years. This review only presents the corresponding reactions of 1,3-enyne structural motifs to provide the functionalized pyridine and pyrrole derivatives. The functionalization reactions cover iodination, bromination, trifluoromethylation, azidation, carbonylation, arylation, alkylation, selenylation, sulfenylation, amidation, esterification, and hydroxylation. We also briefly introduce the applications of the products and the reaction mechanisms for the synthesis of corresponding N-heterocycles.


Molecules ◽  
2019 ◽  
Vol 24 (17) ◽  
pp. 3191 ◽  
Author(s):  
Ting-Bi Hua ◽  
Qing-Qing Yang ◽  
You-Quan Zou

Diazo compounds have proven to be a useful class of carbenes or metal carbenoids sources under thermal, photochemical, or metal-catalyzed conditions, which can subsequently undergo a wide range of synthetically important transformations. Recently, asymmetric photocatalysis has provoked increasing research interests, and great advances have been made in this discipline towards the synthesis of optically enriched compounds. In this context, the past two decades have been the most productive period in the developments of enantioselective photochemical reactions of diazo compounds due to a better understanding of the reactivities of diazo compounds and the emergence of new catalytic modes, as well as easier access to and treatment of stabilized diazo compounds. This review highlights these impressive achievements according to the reaction type, and the general mechanisms and stereochemical inductions are briefly discussed as well.


Fermentation ◽  
2018 ◽  
Vol 4 (3) ◽  
pp. 54 ◽  
Author(s):  
Niël van Wyk ◽  
Heinrich Kroukamp ◽  
Isak Pretorius

Yeast—especially Saccharomyces cerevisiae—have long been a preferred workhorse for the production of numerous recombinant proteins and other metabolites. S. cerevisiae is a noteworthy aroma compound producer and has also been exploited to produce foreign bioflavour compounds. In the past few years, important strides have been made in unlocking the key elements in the biochemical pathways involved in the production of many aroma compounds. The expression of these biochemical pathways in yeast often involves the manipulation of the host strain to direct the flux towards certain precursors needed for the production of the given aroma compound. This review highlights recent advances in the bioengineering of yeast—including S. cerevisiae—to produce aroma compounds and bioflavours. To capitalise on recent advances in synthetic yeast genomics, this review presents yeast as a significant producer of bioflavours in a fresh context and proposes new directions for combining engineering and biology principles to improve the yield of targeted aroma compounds.


2019 ◽  
Vol 16 (1) ◽  
pp. 70-97 ◽  
Author(s):  
Xiaohua Cai ◽  
Mengzhi Yang ◽  
Hui Guo

Background: Enamines and their variant enamides as powerful and versatile synthons have attracted great attention in synthetic chemistry. Enamides display unique stability and reduce enaminic reactivity in view of the electron-withdrawing effect of N-acyl group. A great deal of satisfactory achievements in the synthesis and application of enamides has been made in recent years. Especially, tertiary enamides without N-H bond regarded as low reactivity of compounds in the past can act as excellent nucleophiles to react with electrophiles for the construction of various nitrous molecules. </P><P> Objective: This review focuses on recent advances on tertiary enamides in the synthetic strategies and applications including addition, coupling reaction, functionalization and electro- or photo-chemical reaction. Conclusion: Tertiary enamides as electron-deficient nucleophiles display a satisfactory balance between stability and reactivity to offer multiple opportunities for the construction of various functionalized nitrogencontaining compounds. Further exploration of the reactive mechanisms involved tertiary enamides and the development of novel and efficient transformations to generate ever more complex building blocks starting from tertiary enamides are particularly worth pursuing.


2021 ◽  
Vol 25 ◽  
Author(s):  
Xiao-hua CAI ◽  
Hui GUO

: The development of simple, atom-economical, and sustainable methodologies for the construction of various functional molecules from easily available substrates has been of great interest in synthetic chemistry. N,N-dimethylformamide (DMF) is an inexpensive, abundant solvent and industrial raw material. It is considered as an effective polar solvent and a versatile reagent in synthetic transformations. During the past few decades, many significant and attractive achievements have been made in the fields of DMF as a reactant. The mini-review will mainly summarize recent advances in the applicants of DMF as a multipurpose building block in synthetic reactions.


PEDIATRICS ◽  
1951 ◽  
Vol 8 (5) ◽  
pp. 752-752

This book is divided into 3 portions corresponding to the 3 Porter Lectures given by Dr. Cannon at the University of Kansas. The work described was done by a research team at the University of Chicago. In an interesting and easily understood manner the author discusses new advances made in the field of nutrition over the past 2 decades. The first portion of the monograph is devoted to a brief discussion of earlier data gathered by other investigative groups which contributed to the present work.


2018 ◽  
Vol 90 (4) ◽  
pp. 733-744 ◽  
Author(s):  
Simon Duttwyler

AbstractSignificant progress in the functionalization of icosahedral boron clusters has been made in the past years, leading to an increasing number of applications in various fields of research. The direct conversion of B–H bonds to substituted vertices constitutes an attractive strategy to synthesize cage compounds with desired properties. In this report, recent advances in the transition metal-catalyzed B–H activation of neutral and anionic boron clusters are presented.


Author(s):  
Niël van Wyk ◽  
Heinrich Kroukamp ◽  
Isak S. Pretorius

Abstract: Yeast &ndash; especially Saccharomyces cerevisiae &ndash; have long been a preferred workhorse for the production of numerous recombinant proteins and other metabolites. S. cerevisiae is a noteworthy aroma compound producer, and has also been exploited to produce foreign bioflavour compounds. In the past few years, important strides have been made in unlocking the key elements in the biochemical pathways involved in the production of many aroma compounds. The expression of these biochemical pathways in yeast often involves the manipulation of the host strain to direct the flux towards certain precursors needed for the production of the given aroma compound. This review highlights recent advances in the bioengineering of yeast &ndash; including S. cerevisiae &ndash; to produce aroma compounds and bioflavours. To capitalise on recent advances in synthetic yeast genomics, this review presents yeast as a significant producer of bioflavours in a fresh context and proposes new directions for combining engineering and biology principles to improve the yield of targeted aroma compounds.


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