Synthesis of networked polymer based on ring-opening addition reaction of 1,3-benzoxazine with resorcinol

2012 ◽  
Vol 50 (22) ◽  
pp. 4756-4761 ◽  
Author(s):  
Hiroaki Oie ◽  
Atsushi Mori ◽  
Atsushi Sudo ◽  
Takeshi Endo
2019 ◽  
Vol 23 (12) ◽  
pp. 1284-1306
Author(s):  
Vijai K. Rai ◽  
Fooleswar Verma ◽  
Suhasini Mahata ◽  
Smita R. Bhardiya ◽  
Manorama Singh ◽  
...  

The polymeric graphitic carbon nitride (g-C3N4) has been one of the interesting earth abundant elements. Though g-C3N4 finds application as a photocatalyst, its photocatalytic behaviour is limited because of low efficiency, mainly due to rapid charge recombination. To overcome this problem, several strategies have been developed including doping of metal/non-metal in the cavity of g-C3N4. Moreover, the CoFe2O4 NPs have been used in many organic transformations because of its high surface area and easy separation due to its magnetic nature. This review describes the role of cobalt ferrite as magnetic nanoparticles and metal-doped carbon nitride as efficient heterogeneous catalysts for new carbon-carbon and carbon-hetero atom bond formation followed by heterocyclization. Reactions which involved new catalysts for selective activation of readily available substrates has been reported herein. Since nanoparticles enhance the reactivity of catalyst due to higher catalytic area, they have been employed in various reactions such as addition reaction, C-H activation reaction, coupling reaction, cyclo-addition reaction, multi-component reaction, ring-opening reaction, oxidation reaction and reduction reactions etc. The driving force for choosing this topic is based-on huge number of good publications including different types of spinels/metal doped-/graphitic carbon nitride reported in the literature and due to interest of synthetic community in recent years. This review certainly will represent the present status in organic transformation and for exploring further their catalytic efficiency to new organic transformations involving C-H activation reaction through coupling, cyclo-addition, multi-component, ring-opening, oxidation and reduction reactions.


2007 ◽  
Vol 43 (9) ◽  
pp. 3988-3996 ◽  
Author(s):  
Huey-Ling Chang ◽  
Tsung-Yi Chao ◽  
Chih-Chiang Yang ◽  
Shenghong A. Dai ◽  
Ru-Jong Jeng

2021 ◽  
Author(s):  
Yoshiya Sekiguchi ◽  
Naohiko Yoshikai

<div> <div> <div> <p>We report herein an enantioselective conjugate addition reaction of a zinc homoenolate, catalytically generated via ring opening of a cyclopropanol, to an α,β-unsaturated ketone. The reaction is promoted by a zinc aminoalkoxide catalyst generated from Et2Zn and a chiral β-amino alcohol to afford 1,6- diketones, which undergo, upon heating, intramolecular aldol condensation to furnish highly substituted cyclopentene derivatives with good to high enantioselectivities. The reaction has proved applicable to various 1-substituted cyclopropanols as well as chalcones and related enones. The chiral amino alcohol has proved to enable ligand-accelerated catalysis of the homoenolate generation and its conjugate addition. Positive nonlinear effects and lower reactivity of a racemic catalyst have been observed, which can be attributed to a stable and inactive heterochiral zinc aminoalkoxide dimer. </p> </div> </div> </div>


Synthesis ◽  
2021 ◽  
Author(s):  
Cuiwen Kuang ◽  
Chuanfa Ni ◽  
Yucheng Gu ◽  
Jinbo Hu

A novel nucleophilic reaction between cyclic ethers and benzyl bromides is achieved under photoredox catalysis. The reaction proceeds through a single electron transfer (SET) pathway rather than a common SN2 mechanism. By two steps of reduction and oxidation, a benzyl bromide heterolyzes to give a carbocation and bromide ion under mild conditions, and then a cyclic ether captures both the carbocation and bromide ion to afford the addition product.


2014 ◽  
Vol 34 (9) ◽  
pp. 1857 ◽  
Author(s):  
Dong Yan ◽  
Chao Wu ◽  
Weiguo Yi

2015 ◽  
Vol 6 (3) ◽  
pp. 466-475 ◽  
Author(s):  
Xinyi Liang ◽  
Yujie Liu ◽  
Jian Huang ◽  
Liuhe Wei ◽  
Guowei Wang

Novel barbwire-like graft polymers PEO-g-PCL4 were synthesized by combination of ring opening polymerization (ROP) and Glaser coupling with thiol–yne addition reaction via the “grafting from” strategy.


SynOpen ◽  
2021 ◽  
Author(s):  
Kota Sathish ◽  
Sakkani Nagaraju ◽  
Dhurke Kashinath

A solvent dependent and highly regioselective [3+2]-cycloaddition reaction of isoxazole-styrenes and azomethine imines is reported under catalyst-free conditions furnishing a library of pyrazolone-spirooxindole hybrids. Regioselectivity for the isomeric structures were achieved in good yields by the reaction of isoxazole-styrene (1) and azomethine imine (2) in different solvents and temperature. The developed method was extended for the synthesis of tri-substituted dinitrogen-fused pyrazolones for the using 1,6-Michael addition reaction. Further, the isoxazole moiety was converted into carboxylic acid as a model study via ring opening


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