Enzyme-catalyzed organic synthesis of sucrose and trehalose with in situ regeneration of UDP-Glucose

1990 ◽  
Vol 23 (2) ◽  
pp. 155-170 ◽  
Author(s):  
Sharon L. Haynie ◽  
George M. Whitesides
2020 ◽  
Author(s):  
Aidan Kelly ◽  
Peng-Jui (Ruby) Chen ◽  
Jenna Klubnick ◽  
Daniel J. Blair ◽  
Martin D. Burke

<div> <div> <div> <p>Existing methods for making MIDA boronates require harsh conditions and complex procedures to achieve dehydration. Here we disclose that a pre-dried form of MIDA, MIDA anhydride, acts as both a source of the MIDA ligand and an in situ desiccant to enable a mild and simple MIDA boronate synthesis procedure. This method expands the range of sensitive boronic acids that can be converted into their MIDA boronate counterparts. Further utilizing unique properties of MIDA boronates, we have developed a MIDA Boronate Maker Kit which enables the direct preparation and purification of MIDA boronates from boronic acids using only heating and centrifuge equipment that is widely available in labs that do not specialize in organic synthesis. </p> </div> </div> </div>


2020 ◽  
Vol 24 ◽  
Author(s):  
Wengui Wang ◽  
Shoufeng Wang

Abstract:: Minisci-type reactions have become widely known as reactions that involve the addition of carbon-centered radicals to basic heteroarenes followed by formal hydrogen atom loss. While the originally developed protocols for radical generation remain in active use today, in recent years by a new array of radical generation strategies allow use of a wider variety of radical precursors that often operate under milder and more benign conditions. New transformations based on free radical reactivity are now available to a synthetic chemist looking to utilize a Minisci-type reaction. Radical-generation methods based on photoredox catalysis and electrochemistry, which utilize thermal cleavage or the in situ generation of reactive radical precursors, have become popular approaches. Our review will cover the remarkably literature that has appeared on this topic in recent 5 years, from 2015-01 to 2020-01, in an attempt to provide guidance to the synthetic chemist, on both the challenges that have been overcome and applications in organic synthesis.


2016 ◽  
Vol 7 (1) ◽  
Author(s):  
Hyun Ok Ham ◽  
Zheng Qu ◽  
Carolyn A. Haller ◽  
Brent M. Dorr ◽  
Erbin Dai ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (52) ◽  
pp. 41867-41876 ◽  
Author(s):  
Yang Yu ◽  
Huangzhao Wei ◽  
Li Yu ◽  
Tong Zhang ◽  
Sen Wang ◽  
...  

Organic synthesis is used to investigate the degradation of m-cresol and the intermediates are identified by in situ NMR.


2018 ◽  
Vol 116 ◽  
pp. 57-61 ◽  
Author(s):  
Yao Shi ◽  
Pei Zhang ◽  
Tuotuo Fang ◽  
Erhao Gao ◽  
Fujuan Xi ◽  
...  

2018 ◽  
Vol 249 ◽  
pp. 125-131 ◽  
Author(s):  
M. Farooq ◽  
M.N. Almustapha ◽  
M. Imran ◽  
M.A. Saeed ◽  
John M. Andresen

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