Trapping acrylamide by a Michael addition: A computational study of the reaction between acrylamide and niacin

George Papamokos; Jens Dreyer; Luciano Navarini; Paolo Carloni

doi:10.1002/qua.24610

Trapping acrylamide by a Michael addition: A computational study of the reaction between acrylamide and niacin

International Journal of Quantum Chemistry ◽

10.1002/qua.24610 ◽

2014 ◽

Vol 114 (9) ◽

pp. 553-559 ◽

Cited By ~ 2

Author(s):

George Papamokos ◽

Jens Dreyer ◽

Luciano Navarini ◽

Paolo Carloni

Keyword(s):

Michael Addition ◽

Computational Study

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Computational Study of the Aza-Michael Addition of the Flavonoid (+)-Taxifolin in the Inhibition of β-Amyloid Fibril Aggregation

Chemistry - A European Journal ◽

10.1002/chem.201706072 ◽

2018 ◽

Vol 24 (22) ◽

pp. 5813-5824 ◽

Cited By ~ 2

Author(s):

Tiziana Ginex ◽

Marta Trius ◽

F. Javier Luque

Keyword(s):

Michael Addition ◽

Amyloid Fibril ◽

Computational Study ◽

Β Amyloid ◽

Fibril Aggregation

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Tandem β-Elimination/Hetero-Michael Addition Rearrangement of an N-Alkylated Pyridinium Oxime to an O-Alkylated Pyridine Oxime Ether: An Experimental and Computational Study

The Journal of Organic Chemistry ◽

10.1021/jo5026755 ◽

2015 ◽

Vol 80 (4) ◽

pp. 2165-2173 ◽

Cited By ~ 14

Author(s):

Igor Picek ◽

Robert Vianello ◽

Primož Šket ◽

Janez Plavec ◽

Blaženka Foretić

Keyword(s):

Michael Addition ◽

Computational Study ◽

Oxime Ether

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Observation of a Tricyclic[4.1.0.02,4]heptane During a Michael Addition-Ring Closure Reaction and a Computational Study on Its Mechanism of Formation

The Journal of Organic Chemistry ◽

10.1021/acs.joc.7b02218 ◽

2017 ◽

Vol 82 (23) ◽

pp. 12511-12519 ◽

Cited By ~ 9

Author(s):

Marco Farren-Dai ◽

John R. Thompson ◽

Anna Bernardi ◽

Cinzia Colombo ◽

Andrew J. Bennet

Keyword(s):

Michael Addition ◽

Computational Study ◽

Ring Closure ◽

Mechanism Of Formation

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Cover Feature: Computational Study of the Aza-Michael Addition of the Flavonoid (+)-Taxifolin in the Inhibition of β-Amyloid Fibril Aggregation (Chem. Eur. J. 22/2018)

Chemistry - A European Journal ◽

10.1002/chem.201800498 ◽

2018 ◽

Vol 24 (22) ◽

pp. 5677-5677

Author(s):

Tiziana Ginex ◽

Marta Trius ◽

F. Javier Luque

Keyword(s):

Michael Addition ◽

Amyloid Fibril ◽

Computational Study ◽

Β Amyloid ◽

Fibril Aggregation

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The Origins of the Stereoselectivity and Enantioswitch in the Rare‐Earth‐Catalyzed Michael Addition: A Computational Study

ChemCatChem ◽

10.1002/cctc.201900555 ◽

2019 ◽

Vol 11 (16) ◽

pp. 4036-4042 ◽

Cited By ~ 2

Author(s):

Aya Miyazaki ◽

Miho Hatanaka

Keyword(s):

Rare Earth ◽

Michael Addition ◽

Computational Study ◽

The Rare Earth

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ChemInform Abstract: Stereocontrolled Synthesis of Cyclic Ethers by Intramolecular Hetero- Michael Addition. Part 6. A Computational Study of the Anellation to 2, 3-Disubstituted Tetrahydropyrans.

ChemInform ◽

10.1002/chin.199748167 ◽

2010 ◽

Vol 28 (48) ◽

pp. no-no

Author(s):

M. A. RAMIREZ ◽

J. M. PADRON ◽

J. M. PALAZON ◽

V. S. MARTIN

Keyword(s):

Michael Addition ◽

Computational Study ◽

Cyclic Ethers ◽

Stereocontrolled Synthesis

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Stereocontrolled Synthesis of Cyclic Ethers by Intramolecular Hetero-Michael Addition. 6. A Computational Study of the Annelation to 2,3-Disubstituted Tetrahydropyrans

The Journal of Organic Chemistry ◽

10.1021/jo961925t ◽

1997 ◽

Vol 62 (14) ◽

pp. 4584-4590 ◽

Cited By ~ 29

Author(s):

Miguel A. Ramírez ◽

José M. Padrón ◽

José M. Palazón ◽

Víctor S. Martín

Keyword(s):

Michael Addition ◽

Computational Study ◽

Cyclic Ethers ◽

Stereocontrolled Synthesis

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The origin of diastereoselectivity in the Michael addition reaction: a computational study of the interaction between CH-acidic Schiff base and α,β-unsaturated ketones

Tetrahedron ◽

10.1016/j.tet.2010.04.107 ◽

2010 ◽

Vol 66 (27-28) ◽

pp. 5168-5172 ◽

Cited By ~ 4

Author(s):

S. Ilieva ◽

D. Cheshmedzhieva ◽

D. Tasheva

Keyword(s):

Schiff Base ◽

Michael Addition ◽

Addition Reaction ◽

Computational Study ◽

Michael Addition Reaction ◽

Unsaturated Ketones ◽

The Michael Addition

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Fatty acid ketodienes and fatty acid ketotrienes: Michael addition acceptors that accumulate in wounded and diseased Arabidopsis leaves

The Plant Journal ◽

10.1046/j.1365-313x.2000.00897.x ◽

2000 ◽

Vol 24 (4) ◽

pp. 467-476 ◽

Cited By ~ 127

Author(s):

Sabine Vollenweider ◽

Hans Weber ◽

Stephanie Stolz ◽

Aurore Chetelat ◽

Edward E. Farmer

Keyword(s):

Fatty Acid ◽

Michael Addition

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Computational studies on geopolymer catalyst for Michael addition reaction

10.1021/scimeetings.0c05563 ◽

2020 ◽

Author(s):

Uppari Naveena

Keyword(s):

Michael Addition ◽

Addition Reaction ◽

Computational Studies ◽

Michael Addition Reaction

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