One‐Step Solvent‐Free Synthesis of Polyglycolic Acid from Sustainable C1 Feedstocks

2020 ◽  
pp. 2000284
Author(s):  
Yusuf Reyhanoglu ◽  
Berkant Kalayci ◽  
Ersen Gokturk
2018 ◽  
Vol 20 (20) ◽  
pp. 4738-4745 ◽  
Author(s):  
D. S. Wunschik ◽  
K. N. Ingenbosch ◽  
M. Zähres ◽  
J. Horst ◽  
C. Mayer ◽  
...  

An enzymatically controlled one-step synthesis of a non-isocyanate polyurethane monomer from sustainable resources is feasible under mild reaction conditions.


2008 ◽  
Vol 18 (11) ◽  
pp. 1641-1653 ◽  
Author(s):  
Sayan Bhattacharyya ◽  
Ilana Perelshtein ◽  
Ofer Moshe ◽  
Daniel H. Rich ◽  
Aharon Gedanken

ARKIVOC ◽  
2010 ◽  
Vol 2010 (2) ◽  
pp. 315-322
Author(s):  
Filip Bureš ◽  
Jiří Kulhánek ◽  
Miroslav Ludwig

2018 ◽  
Vol 201 ◽  
pp. 438-445 ◽  
Author(s):  
Yi Lu ◽  
Yaling Jia ◽  
Yang Zhou ◽  
Jie Zou ◽  
Guangxian Zhang ◽  
...  

ChemInform ◽  
2007 ◽  
Vol 38 (9) ◽  
Author(s):  
E. S. Putilova ◽  
N. A. Troitskii ◽  
S. G. Zlotin ◽  
O. G. Khudina ◽  
Ya. V. Burgart ◽  
...  

2016 ◽  
Vol 181 ◽  
pp. 363-370 ◽  
Author(s):  
Nataliya V. Maksimchuk ◽  
Irina D. Ivanchikova ◽  
Artem B. Ayupov ◽  
Oxana A. Kholdeeva

2018 ◽  
Vol 30 (10) ◽  
pp. 2421-2426 ◽  
Author(s):  
Garrhett G. Via ◽  
Chelsea L. Shugart ◽  
Sophia L. Melnyk ◽  
Stephanie R. Hupman ◽  
Kristin K. Cline

2010 ◽  
Vol 14 (07) ◽  
pp. 621-629 ◽  
Author(s):  
Shabnam Nia ◽  
Xianchang Gong ◽  
Charles Michael Drain ◽  
Matthew Jurow ◽  
Waqar Rizvi ◽  
...  

The scope and optimization of a solvent-free method for the rapid preparation and facile purification of technologically important meso-substituted aryl porphyrins, such as 5,10,15,20-tetraphenylporphyrin is presented. This one-step method involves heating the aromatic aldehyde to ~200°C in a vial fitted with a septum-lined cap, followed by addition of the pyrrole and maintaining the temperature for about 20 minutes. The dioxygen in air serves as the oxidant. Present results show that the addition of benzoic acid as a catalyst improves the yield of 5,10,15,20-tetraphenylporphyrin from 22% to 32% and of para halogenated phenylporphyrins from 10% to ~25%. Herein is also presented an examination of the many factors that influence the yield, the ease of purification, and the ability to scale up the reaction. Since the tarry by-products from this method are much less soluble than in most other synthetic strategies, much less solvent is required for purification; simple extraction is often sufficient. This method can be scaled in the lab to > 300 mg, and provides an attractive route to many meso-substituted porphyrins because of its minimal waste generation in terms of both solvent and chromatography support.


2016 ◽  
Vol 13 (9) ◽  
pp. 1571-1577 ◽  
Author(s):  
Hassan Zali-Boeini ◽  
Seyed Gholamhossein Mansouri

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