ChemInform Abstract: Copper(I)/Lewis Acid Triggered Ring-Opening Coupling Reaction of Cyclopropenes with Nitriles.

ChemInform ◽  
2015 ◽  
Vol 46 (31) ◽  
pp. no-no
Author(s):  
Huawen Huang ◽  
Xiaochen Ji ◽  
Fuhong Xiao ◽  
Guo-Jun Deng
Keyword(s):  
Lewis Acid ◽  
Ring Opening ◽  
Coupling Reaction

Copper(i)/Lewis acid triggered ring-opening coupling reaction of cyclopropenes with nitriles

RSC Advances ◽  
2015 ◽  
Vol 5 (33) ◽  
pp. 26335-26338 ◽  
Author(s):  
Huawen Huang ◽  
Xiaochen Ji ◽  
Fuhong Xiao ◽  
Guo-Jun Deng
Keyword(s):  
Lewis Acid ◽  
Ring Opening ◽  
Coupling Reaction ◽  
Facile Synthesis

A ring-opening coupling reaction of D–A cyclopropenes and nitriles is described for the facile synthesis of γ-amino ketones.

Convergent Synthesis of Immune Inhibitor IMMH002

Synthesis ◽  
2020 ◽  
Author(s):  
Qiong Xiao ◽  
Si Chen ◽  
Zeyu Shi ◽  
Dali Yin
Keyword(s):  
Environmental Impact ◽  
Lewis Acid ◽  
Column Chromatography ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Convergent Synthesis ◽  
Quality Problem ◽  
Cross Coupling Reaction

AbstractA convergent synthesis of IMMH002 in 36% overall yield starting from bromobenzene is described with a key Suzuki–Miyaura cross-coupling reaction used to provide a crucial intermediate. The route does not require column chromatography and solves the most intractable quality problem caused by a homologue by-product in the original linear synthesis. Furthermore, reducing the use of Lewis acid mediated reactions improves the environmental impact of the synthesis and reduces overall waste. The new route described herein is more efficient, convenient, reliable, and economically more viable when compared to the previously reported linear route.

Design and synthesis of 1,8-Naphthalimide Functionalized Benzothiadiazoles

2021 ◽  
Author(s):  
Rajneesh Misra ◽  
Yogjivan Rout
Keyword(s):  
Ring Opening ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Design And Synthesis ◽  
Cross Coupling Reaction ◽  
Ring Opening Reaction

A series of multi acceptor based push-pull derivatives BTD2–BTD5 were designed and synthesized via Pd-catalyzed Sonogashira cross-coupling reaction followed by [2+2] cycloaddition–electrocyclic ring-opening reaction in which benzothiadiazole (BTD, A1), naphthalimide...

Cross‐Coupling Reaction of Alkenyl Sulfoximines and Alkenyl Aminosulfoxonium Salts with Organozincs by Dual Nickel Catalysis and Lewis Acid Promotion

2019 ◽  
Vol 25 (35) ◽  
pp. 8371-8386 ◽  
Author(s):  
Irene Erdelmeier ◽  
Gerd Bülow ◽  
Chang‐Wan Woo ◽  
Jürgen Decker ◽  
Gerhard Raabe ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Nickel Catalysis ◽  
Cross Coupling Reaction

scholarly journals Development of Inherently Flame—Retardant Phosphorylated PLA by Combination of Ring-Opening Polymerization and Reactive Extrusion

Materials ◽  
2019 ◽  
Vol 13 (1) ◽  
pp. 13 ◽  
Author(s):  
Rosica Mincheva ◽  
Hazar Guemiza ◽  
Chaimaa Hidan ◽  
Sébastien Moins ◽  
Olivier Coulembier ◽  
...  
Keyword(s):  
Heat Release ◽  
Flame Retardant ◽  
Ring Opening ◽  
Coupling Reaction ◽  
Reactive Extrusion ◽  
Ring Opening Polymerization ◽  
Hexamethylene Diisocyanate ◽  
Cone Calorimetry ◽  
Loss Cone ◽  
Ul 94

In this study, a highly efficient flame-retardant bioplastic poly(lactide) was developed by covalently incorporating flame-retardant DOPO, that is, 9,10-dihydro-oxa-10-phosphaphenanthrene-10-oxide. To that end, a three-step strategy that combines the catalyzed ring-opening polymerization (ROP) of L,L-lactide (L,L-LA) in bulk from a pre-synthesized DOPO-diamine initiator, followed by bulk chain-coupling reaction by reactive extrusion of the so-obtained phosphorylated polylactide (PLA) oligomers (DOPO-PLA) with hexamethylene diisocyanate (HDI), is described. The flame retardancy of the phosphorylated PLA (DOPO-PLA-PU) was investigated by mass loss cone calorimetry and UL-94 tests. As compared with a commercially available PLA matrix, phosphorylated PLA shows superior flame-retardant properties, that is, (i) significant reduction of both the peak of heat release rate (pHRR) and total heat release (THR) by 35% and 36%, respectively, and (ii) V0 classification at UL-94 test. Comparisons between simple physical DOPO-diamine/PLA blends and a DOPO-PLA-PU material were also performed. The results evidenced the superior flame-retardant behavior of phosphorylated PLA obtained by a reactive pathway.

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