Recent Developments in Synthetic Chemistry, Chiral Separations, and Applications ofTröger's Base Analogues

2009 ◽  
Vol 92 (3) ◽  
pp. 415-444 ◽  
Author(s):  
Sergey Sergeyev
2013 ◽  
Vol 42 (44) ◽  
pp. 15540 ◽  
Author(s):  
Maryline Ferrier ◽  
William M. Kerlin ◽  
Frederic Poineau ◽  
Alfred P. Sattelberger ◽  
Kenneth R. Czerwinski

2006 ◽  
Vol 34 (2) ◽  
pp. 301-303 ◽  
Author(s):  
J.M. Woodley

The design of biocatalytic processes for industrial synthetic chemistry is determined in large part by the choice of isolated enzyme or whole-cell catalyst form. In the present paper, the considerations for choice are identified and some important classes of bioconversion are discussed in relation to the choice to be made. Recent developments in cell and protein engineering as well as reactor and process engineering are discussed in addition.


Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4322
Author(s):  
Cuong Viet Bui ◽  
Thomas Rosenau ◽  
Hubert Hettegger

Polysaccharides, oligosaccharides, and their derivatives, particularly of amylose, cellulose, chitosan, and β-cyclodextrin, are well-known chiral selectors (CSs) of chiral stationary phases (CSPs) in chromatography, because they can separate a wide range of enantiomers. Typically, such CSPs are prepared by physically coating, or chemically immobilizing the polysaccharide and β-cyclodextrin derivatives onto inert silica gel carriers as chromatographic support. Over the past few years, new chiral selectors have been introduced, and progressive methods to prepare CSPs have been exploited. Also, chiral recognition mechanisms, which play a crucial role in the investigation of chiral separations, have been better elucidated. Further insights into the broad functional performance of commercially available chiral column materials and/or the respective newly developed chiral phase materials on enantiomeric separation (ES) have been gained. This review summarizes the recent developments in CSs, CSP preparation, chiral recognition mechanisms, and enantiomeric separation methods, based on polysaccharides and β-cyclodextrins as CSs, with a focus on the years 2019–2020 of this rapidly developing field.


2006 ◽  
Vol 78 (10) ◽  
pp. 1823-1834 ◽  
Author(s):  
Hiroshi Sugimoto ◽  
Shohei Inoue

The alternating copolymerization of carbon dioxide and epoxide to give polycarbonate has attracted the attention of many chemists, because it is one of the most promising methodologies for the utilization of carbon dioxide as a safe, clean, and abundant raw material in the synthetic chemistry. Recent developments of the catalysts for the alternating copolymerization are based on the rational design of metal complexes, especially complexes of transition metal with well-defined structures.


Synlett ◽  
2020 ◽  
Vol 31 (18) ◽  
pp. 1753-1759
Author(s):  
Da-Zhen Xu ◽  
Ren-Ming Hu ◽  
Yi-Huan Lai

The direct functionalization of C(sp3)–H bonds is an attractive research topic in organic synthetic chemistry. The cross-dehydrogenative coupling (CDC) reaction provides a simple and powerful tool for the construction of C–C and C–heteroatom bonds. Recently, some progress has been made in the iron-catalyzed aerobic oxidative CDC reactions. Here, we present recent developments in the direct functionalization of C(sp3)–H bonds catalyzed by simple iron salts with molecular oxygen as the terminal oxidant.1 Introduction2 C(sp3)–C Bond Formation3 C(sp3)–N Bond Formation4 C(sp3)–S(Se) Bond Formation5 Conclusion and Outlook


2019 ◽  
Vol 131 (8) ◽  
Author(s):  
Muhammad Faisal ◽  
Aamer Saeed ◽  
Sarwat Hussain ◽  
Parsa Dar ◽  
Fayaz Ali Larik

2018 ◽  
pp. 607-629 ◽  
Author(s):  
Roberta Franzini ◽  
Alessia Ciogli ◽  
Francesco Gasparrini ◽  
Omar H. Ismail ◽  
Claudio Villani

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