scholarly journals On the outside looking in: rethinking the molecular mechanism of 1,3-dipolar cycloadditions from the perspective of bonding evolution theory. The reaction between cyclic nitrones and ethyl acrylate

2017 ◽  
Vol 19 (28) ◽  
pp. 18288-18302 ◽  
Author(s):  
A. I. Adjieufack ◽  
I. M. Ndassa ◽  
I. Patouossa ◽  
J. K. Mbadcam ◽  
V. S. Safont ◽  
...  
Keyword(s):  
Molecular Mechanism ◽  
Ethyl Acrylate ◽  
Evolution Theory ◽  
Dipolar Cycloadditions ◽  
Cyclic Nitrones

Understanding the molecular mechanism of 1,3-dipolar cycloadditions using the bonding evolution theory.

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

Use of highly stereospecific 1,3-dipolar cycloadditions of cyclic nitrones with acetylenes in the preparation of novel heterocyclic ring systems

1997 ◽  
pp. 155-162 ◽  
Author(s):  
W. Russell Bowman ◽  
Roy V. Davies ◽  
Alexandra M. Z. Slawin ◽  
Gian S. Sohal ◽  
Roger B. Titman ◽  
...  
Keyword(s):  
Heterocyclic Ring ◽  
Ring Systems ◽  
Dipolar Cycloadditions ◽  
Cyclic Nitrones

ChemInform Abstract: 1,3-Dipolar Cycloadditions of New 2,5-Bifunctionalized Five-Membered Cyclic Nitrones.

ChemInform ◽  
2012 ◽  
Vol 43 (35) ◽  
pp. no-no
Author(s):  
Marian Buchlovic ◽  
Simona Hebanova ◽  
Milan Potacek
Keyword(s):  
Dipolar Cycloadditions ◽  
Cyclic Nitrones

1,3-Dipolar cycloadditions of new 2,5-bifunctionalized five-membered cyclic nitrones

Tetrahedron ◽  
2012 ◽  
Vol 68 (14) ◽  
pp. 3117-3122 ◽  
Author(s):  
Marian Buchlovič ◽  
Simona Hebanová ◽  
Milan Potáček
Keyword(s):  
Dipolar Cycloadditions ◽  
Cyclic Nitrones

A DFT study of 1,3-dipolar cycloadditions of cyclic nitrones to unsaturated lactones. Part II

2008 ◽  
Vol 19 (18) ◽  
pp. 2140-2148 ◽  
Author(s):  
Sebastian Stecko ◽  
Konrad Paśniczek ◽  
Carine Michel ◽  
Anne Milet ◽  
Serge Perez ◽  
...  
Keyword(s):  
Dft Study ◽  
Dipolar Cycloadditions ◽  
Cyclic Nitrones ◽  
Unsaturated Lactones

scholarly journals How effectively bonding evolution theory retrieves and visualizes curly arrows: The cycloaddition reaction of cyclic nitrones

2019 ◽  
Vol 119 (19) ◽  
Author(s):  
Abel I. Adjieufack ◽  
Maraf Mbah Bake ◽  
Joseph Ketcha Mbadcam ◽  
Ibrahim Mbouombouo Ndassa ◽  
Juan Andrés ◽  
...  
Keyword(s):  
Cycloaddition Reaction ◽  
Evolution Theory ◽  
Cyclic Nitrones

1,3-Dipolar cycloadditions of cyclic nitrones to γ-bromo α,β-unsaturated esters and lactones

Tetrahedron ◽  
1998 ◽  
Vol 54 (24) ◽  
pp. 6947-6956 ◽  
Author(s):  
Pedro de March ◽  
Marta Figueredo ◽  
Josep Font ◽  
Antonio Salgado
Keyword(s):  
Unsaturated Esters ◽  
Dipolar Cycloadditions ◽  
Cyclic Nitrones

1,3-Dipolar cycloadditions of ylide of 5-nitro-2-furfurylpyridinium bromide in indolizine synthesis

1982 ◽  
Vol 47 (6) ◽  
pp. 1738-1745 ◽  
Author(s):  
Jarmila Štetinová ◽  
Miloslava Dandárová ◽  
Jaroslav Kováč ◽  
Darina Mesárošová ◽  
Ján Leško
Keyword(s):  
Mass Spectra ◽  
Cycloaddition Reaction ◽  
Ethyl Acrylate ◽  
Dipolar Cycloaddition ◽  
Dimethyl Acetylenedicarboxylate ◽  
Diethyl Maleate ◽  
Dipolar Cycloadditions ◽  
H Nmr

Substituted 3-(5-nitro-2-furyl)indolizines III-X were synthesized by 1,3-dipolar cycloaddition reaction of the ylide II, generated from 5-nitro-2-furfurylpyridinium bromide (I), with acrylonitrile, ethyl acrylate, diethyl maleate, benzalacetophenone, ethyl 3-(5-nitro-2-furyl)acrylate, (5-nitro-2-furfurylidene)acetophenone, β-nitrostyrene and dimethyl acetylenedicarboxylate. The structure of these products is discussed on the basis of their 1H NMR and mass spectra.

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