Acceleration of 1,3-Dipolar Cycloadditions by Integration of Strain and Electronic Tuning

2021 ◽  
Author(s):  
Jesús M. Dones ◽  
Nile S. Abularrage ◽  
Namrata Khanal ◽  
Brian Gold ◽  
Ronald T. Raines
Keyword(s):  
Dipolar Cycloadditions ◽  
Electronic Tuning

scholarly journals Surface Modification of Black Phosphorus with Group 13 Lewis Acids for Ambient Protection and Electronic Tuning

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Author(s):  
Daniel Tofan ◽  
Yukako Sakazaki ◽  
Kendahl Walz Mitra ◽  
Ruoming Peng ◽  
Seokhyeong Lee ◽  
...  
Keyword(s):  
Surface Modification ◽  
Lewis Acids ◽  
Black Phosphorus ◽  
Group 13 ◽  
Electronic Tuning

Phosphate-modified Co-Ni phosphide heterostructure formed by interfacial and electronic tuning for boosted faradaic properties

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Author(s):  
Zhan Li ◽  
Hongyu Mi ◽  
Chenchen Ji ◽  
Fengjiao Guo ◽  
Pengtao Qiu ◽  
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Keyword(s):  
Electronic Properties ◽  
Electrode Materials ◽  
Physicochemical Characteristics ◽  
Compositional Modulation ◽  
Electronic Tuning

The rationally structural and compositional modulation endows electrode materials with unique physicochemical characteristics owing to their adjustable electronic properties. Herein, a phosphate-modified hierarchical nanoarray consisting of heterojunction with well-aligned cobalt...

Substituent and solvent effects in the 1,3-dipolar cycloadditions for synthesis of anti-influenza agent peramivir and its analog

Tetrahedron ◽  
2019 ◽  
Vol 75 (33) ◽  
pp. 4458-4470
Author(s):  
Chien-Liang Chen ◽  
Tzu-Wei Chiu ◽  
Yung-Wen Chen ◽  
Jim-Min Fang
Keyword(s):  
Solvent Effects ◽  
Dipolar Cycloadditions

1,3-Dipolar cycloadditions of Arylcarbonitrile Oxides and Diaryl Nitrilimines with Some 2-Arylmethylene-1,3-Indanediones; regiochemistry of the Reactions

2003 ◽  
Vol 2003 (4) ◽  
pp. 204-207 ◽  
Author(s):  
Sarra Boudriga ◽  
Mohiedinne Askri ◽  
Rafik Gharbi ◽  
Mohamed Rammah ◽  
Kabula Ciamala
Keyword(s):  
Ring Closure ◽  
Dipolar Cycloaddition ◽  
Dipolar Cycloadditions

Ring-closure reaction affording spiroisoxazolines and spiropyrazolines via a 1,3-dipolar cycloaddition between the title compounds, occurs with high regioselectivity.

ChemInform Abstract: Macrocyclic Heterophanes via Intramolecular 1,3-Dipolar Cycloadditions

ChemInform ◽  
2010 ◽  
Vol 30 (16) ◽  
pp. no-no
Author(s):  
Giorgio Molteni ◽  
Gaetano Zecchi
Keyword(s):  
Dipolar Cycloadditions

Stereospecificity of 1,.3-dipolar cycloadditions of cyclic nitrones to (E) and (Z)-β-nitrostyrenes

Tetrahedron ◽  
1987 ◽  
Vol 43 (8) ◽  
pp. 1835-1846 ◽  
Author(s):  
Marina Burdisso ◽  
Anna Gamba ◽  
Remo Gandolfi ◽  
Paolo Pevarello
Keyword(s):  
Dipolar Cycloadditions ◽  
Cyclic Nitrones

ChemInform Abstract: 1,3-Dipolar Cycloadditions of Cyclic Nitrones to γ-Bromo α,β-Unsaturated Esters and Lactones.

ChemInform ◽  
2010 ◽  
Vol 29 (41) ◽  
pp. no-no
Author(s):  
P. DE MARCH ◽  
M. FIGUEREDO ◽  
J. FONT ◽  
A. SALGADO
Keyword(s):  
Unsaturated Esters ◽  
Dipolar Cycloadditions ◽  
Cyclic Nitrones

1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity, through 1,3-Dipolar Cycloadditions

2014 ◽  
Vol 2014 (16) ◽  
pp. 3289-3306 ◽  
Author(s):  
Antonino Lauria ◽  
Riccardo Delisi ◽  
Francesco Mingoia ◽  
Alessio Terenzi ◽  
Annamaria Martorana ◽  
...  
Keyword(s):  
Biological Activity ◽  
Heterocyclic Compounds ◽  
Dipolar Cycloadditions
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