Enzyme mediated silicon–oxygen bond formation; the use of Rhizopus oryzae lipase, lysozyme and phytase under mild conditions

2010 ◽  
Vol 39 (39) ◽  
pp. 9361 ◽  
Author(s):  
Vincenzo Abbate ◽  
Alan R. Bassindale ◽  
Kurt F. Brandstadt ◽  
Rachel Lawson ◽  
Peter G. Taylor
2005 ◽  
Vol 8 (12) ◽  
pp. 1082-1084 ◽  
Author(s):  
Kaustavmoni Deka ◽  
Rupam Jyoti Sarma ◽  
Jubaraj B. Baruah

2011 ◽  
Vol 105 (2) ◽  
pp. 268-275 ◽  
Author(s):  
Vincenzo Abbate ◽  
Alan R. Bassindale ◽  
Kurt F. Brandstadt ◽  
Peter G. Taylor

1990 ◽  
Vol 43 (3) ◽  
pp. 511 ◽  
Author(s):  
KM Downard ◽  
JH Bowie ◽  
RN Hayes

Trimethylsilyl anions containing additional alkoxy, ketone or carboxylic acid funtionality undergo a variety of rearrangement reactions upon collisional activation. The most common are those which involve production of Si -O bonds, either by formation of Me3SiO- or by elimination of Me3SiOH.


Author(s):  
Ayesha Jalil ◽  
Yaxin O Yang ◽  
Zhendong Chen ◽  
Rongxuan Jia ◽  
Tianhao Bi ◽  
...  

: Hypervalent iodine reagents are a class of non-metallic oxidants have been widely used in the construction of several sorts of bond formations. This surging interest in hypervalent iodine reagents is essentially due to their very useful oxidizing properties, combined with their benign environmental character and commercial availability from the past few decades ago. Furthermore, these hypervalent iodine reagents have been used in the construction of many significant building blocks and privileged scaffolds of bioactive natural products. The purpose of writing this review article is to explore all the transformations in which carbon-oxygen bond formation occurred by using hypervalent iodine reagents under metal-free conditions


2020 ◽  
Vol 02 (03) ◽  
pp. e128-e132
Author(s):  
Shao-Zheng Guo ◽  
Zhi-Qun Yu ◽  
Wei-Ke Su

AbstractThe development of highly efficient C–C bond formation methods for the synthesis of ethyl 2-(2,4-dichloro-5-fluorobenzoyl)-3-(dimethylamino)acrylate 1 in continuous flow processes has been described, which is based on the concept of rapid and efficient activation of carboxylic acid. 2,4-Dichloro-5-fluorobenzoic acid is rapidly converted into highly reactive 2,4-dichloro-5-fluorobenzoyl chloride by treating with inexpensive and less-toxic solid bis(trichloromethyl)carbonate. And then it rapidly reacts with ethyl 3-(dimethylamino)acrylate to afford the desired 1. This process can be performed under mild conditions. Compared with the traditional tank reactor process, less raw material consumption, higher product yield, less reaction time, higher operation safety ensured by more the environmentally friendly procedure, and process continuity are achieved in the continuous-flow system.


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