ChemInform Abstract: Hetero-Diels-Alder Reaction of Substituted 1-Oxabutadienes and 2-Ethoxyvinyl Acetate. An Entry to Various Natural Occurring Carbohydrates.

ChemInform ◽  
1990 ◽  
Vol 21 (52) ◽  
Author(s):  
L. F. TIETZE ◽  
U. HARTFIEL
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Substituted 1

SUBSTITUTED 1-THIA-3-AZA -1,3-BUTADIENE: DIELS-ALDER REACTION WITH METHYLACRYLATE. DETERMINATION OF ACTIVATION PARAMETERS

1989 ◽  
Vol 42 (1-2) ◽  
pp. 15-19 ◽  
Author(s):  
Moustafa Chehna ◽  
Jean Paul Pradere ◽  
Herve Quiniou ◽  
Denis Le Botlan ◽  
Loic Toupet
Keyword(s):  
Activation Parameters ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Substituted 1

ChemInform Abstract: π-Facial Selectivity in the Diels-Alder Reaction of 5-Substituted 1, 3-Cyclopentadienes.

ChemInform ◽  
2010 ◽  
Vol 25 (8) ◽  
pp. no-no
Author(s):  
M. ISHIDA ◽  
T. AOYAMA ◽  
Y. BENIYA ◽  
S. YAMABE ◽  
S. KATO ◽  
...  
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Facial Selectivity ◽  
Substituted 1

The Diels-Alder Reaction of 2-Ethenyl-1,4-Benzodioxin: A New and Simple Synthesis of Bisaryl Ethers

Synlett ◽  
1989 ◽  
Vol 1989 (01) ◽  
pp. 30-32
Author(s):  
Thomas V. Lee ◽  
Alistair J. Leigh ◽  
Christopher B. Chapleo
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Simple Synthesis ◽  
Diels Alder Reaction

The intermolecular anthracene-transfer in a regiospecific antipodal C60 difunctionalization

2020 ◽  
Author(s):  
Radu Talmazan ◽  
Klaus R. Liedl ◽  
Bernhard Kräutler ◽  
Maren Podewitz
Keyword(s):  
Noncovalent Interactions ◽  
Interaction Model ◽  
Alder Reaction ◽  
Diels Alder ◽  
Stacking Interactions ◽  
Pi Stacking ◽  
Diels Alder Reaction ◽  
Double Decker ◽  
Anthracene Molecule ◽  
New Strategies

We analyze the mechanism of the topochemically controlled difunctionalization of C60 and anthracene, where an anthracene molecule is transferred from one C60 monoadduct to another one under exclusive formation of equal amounts of C60 and the difficult to make antipodal C60 bisadduct. Our herein disclosed dispersion corrected DFT studies show the anthracene transfer to take place in a synchronous retro Diels-Alder/Diels-Alder reaction: an anthracene molecule dissociates from one fullerene under formation of an intermediate, while already undergoing stabilizing interactions with both neighboring fullerenes, facilitating the reaction kinetically. In the intermediate, a planar anthracene molecule is sandwiched between two neighboring fullerenes and forms equally strong "double-decker" type pi-pi stacking interactions with both of these fullerenes. Analysis with the distorsion interaction model shows that the anthracene unit of the intermediate is almost planar with minimal distorsions. This analysis sheds light on the existence of noncovalent interactions engaging both faces of a planar polyunsaturated ring and two convex fullerene surfaces in an unprecedented 'inverted sandwich' structure. Hence, it sheds light on new strategies to design functional fullerene based materials.<br>

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