Gradient Copolymer Prepared from Alternating Ring-Opening Metathesis of Three Monomers

2021 ◽  
Author(s):  
Francis Opoku Boadi ◽  
Nicole S Sampson

Bicyclo[4.2.0]oct-6-ene-7-carboxamide is a simple but highly strained olefin monomer which forms an alternating copolymer with cyclohexene in the presence of N-heterocyclic carbene-ruthenium catalyst. [4.2.0] moiety with bulky substituent on C7...

2021 ◽  
Vol 63 ◽  
pp. 152712
Author(s):  
Daichi Yoshida ◽  
Garry Sinawang ◽  
Motofumi Osaki ◽  
Hiroyasu Yamaguchi ◽  
Akira Harada ◽  
...  

2016 ◽  
Vol 14 (25) ◽  
pp. 6079-6087 ◽  
Author(s):  
Benjamin J. Lidster ◽  
Dharam R. Kumar ◽  
Andrew M. Spring ◽  
Chin-Yang Yu ◽  
Madeleine Helliwell ◽  
...  

Highly strained alkyl-substituted [2.2]paracyclophane-1,9-dienes, suitable for ring opening metathesis polymerization to poly(phenylene vinylenes), have been prepared in excellent yields.


2020 ◽  
Author(s):  
Sepand Nistanaki ◽  
Hosea Nelson

We report the utility of readily available heterocycles as precursors to unique ring-opening metathesis polymerization (ROMP) monomers. Photochemical valence isomerization reactions of pyridones, dihydropyridines, and pyrones dearomatize the parent heterocycles to their highly strained Dewar isomers, which readily engage in controlled ROMP reactions using Grubbs catalysts. This strategy is used to access novel polymer backbones that contain strained β-lactam and azetidine cores, which can be further derivatized using post-polymerization chemistries. We demonstrate this through the synthesis of water-soluble β-amino acid polymers and soluble poly(acetylene) derivatives.


2021 ◽  
Author(s):  
Kuppan Ramachandran ◽  
Pazhamalai Anbarasan

Cyclopropenes are highly strained three-membered carbocycle, which offers unique reactivity in organic synthesis. Herein, Cp*CoIII-catalyzed ring-opening isomerization of cyclopropenes to cobalt vinylcarbene has been utilized for the synthesis of multisubstituted...


Synthesis ◽  
2021 ◽  
Author(s):  
Yujin Jang ◽  
Roger Machin-Rivera ◽  
Vincent Lindsay

Cyclopropanone derivatives constitute highly strained cycloalkanones with promising applications as three-carbon building blocks in organic synthesis. Due to the presence of a ketone in such a small ring system, all C–C bonds and the carbonyl group are considered to be labile in suitable conditions, leading to a wide variety of synthetic disconnections, including nucleophilic addition, ring expansion, ring-opening and (formal) cycloaddition. Despite their synthetic potential, the widespread adoption of cyclopropanones as substrates has been considerably hampered by the difficulties associated with the preparation and storage of such unstable compounds, prompting the development of cyclopropanone surrogates that can equilibrate to parent ketone in situ via elimination. This review summarizes the syntheses and applications of cyclopropanone derivatives and their equivalents, and offers a perspective of the state of the field as well as its expected future directions.


2007 ◽  
Vol 39 (4) ◽  
pp. 318-329 ◽  
Author(s):  
Yasushi Nishihara ◽  
Yoshiaki Inoue ◽  
Akira T Saito ◽  
Yuushou Nakayama ◽  
Takeshi Shiono ◽  
...  

1997 ◽  
Vol 124 (1) ◽  
pp. 561-565 ◽  
Author(s):  
Derek P. Gates ◽  
Ron Rulkens ◽  
Regina Dirk ◽  
Paul Nguyen ◽  
John K. Pudelski ◽  
...  
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