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Wesley Chalifoux

Chemiker

Name	Wesley Chalifoux
Zeit	2006- (Wirkungsdaten)
Ort	USA Kanada
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Chemiker (charakteristischer Beruf) Hochschullehrer
Variante	Wesley A. Chalifoux
Beziehung	University of Alberta University of Nevada, Reno
Quelle	https://wchalifoux.wixsite.com/researchgroup/wesley-a-chalifoux (Stand: 23.02.2024)
Datensatztyp	Person
GND-Nummer	1275992757
Datensatz-ID	1275992757
Beteiligt an alle anzeigen Chiral Teropyrenes: Synthesis, Structure, and Spectroscopic Studies Chiral Teropyrenes: Synthesis, Structure, and Spectroscopic Studies Dissymmetrical chiral peropyrenes: synthesis via iridium-catalyzed C–H activation/alkyne benzannulation and study of their properties π‐Extended Helical Nanographenes: Synthesis and Photophysical Properties of Naphtho (1,2‐ a) pyrenes ** Synthesis and Structure of a Strained, Cyclic meta ‐Quaterphenylene Acetylene Cover Feature: Synthesis and Structure of a Strained, Cyclic meta ‐Quaterphenylene Acetylene (Eur. J. Org. Chem. 28/2019) Synthesis of Dihydroisobenzofuran Carboxaldehyde Derivatives by a Silver‐Catalyzed Sequential Protodesilylation/Cyclization/Oxidation Reaction Synthesis, Structure, Photophysical Properties, and Photostability of Benzodipyrenes Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes Innentitelbild: Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes (Angew. Chem. 45/2018) Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes Inside Cover: Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes (Angew. Chem. Int. Ed. 45/2018) Rapid π-Extension of Aromatics via Alkyne Benzannulations Die Synthese von nichtplanaren, helikalen Graphen‐Nanobändern The Synthesis of Non‐planar, Helically Coiled Graphene Nanoribbons Synthesis of 2-Alkynyl-1,4-cyclohexadienes via a Diels–Alder Reaction of Conjugated 2,4-Diynones Multicomponent Double Diels–Alder/Nazarov Tandem Cyclization of Symmetric Cross‐Conjugated Diynones to Generate (6‐5‐6) Tricyclic Products Pyrenes, Peropyrenes, and Teropyrenes: Synthesis, Structures, and Photophysical Properties Pyrenes, Peropyrenes, and Teropyrenes: Synthesis, Structures, and Photophysical Properties ChemInform Abstract: Highly Regio‐ and Diastereoselective Formation of Tetrasubstituted (Z)‐1,2‐Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl. Photogenerated cumulenic structure of adamantyl endcapped linear carbon chains: An experimental and computational investigation based on infrared spectroscopy ChemInform Abstract: Toward Carbyne: Synthesis and Stability of Really Long Polyynes Polyine mit tert ‐Butyl‐Endgruppen: kristallographischer Nachweis einer reduzierten Bindungslängenalternanz † tert ‐Butyl‐End‐Capped Polyynes: Crystallographic Evidence of Reduced Bond‐Length Alternation † tert ‐Butyl‐End‐Capped Polyynes: Crystallographic Evidence of Reduced Bond‐Length Alternation † Tris (biphenyl‐4‐yl) silyl‐Endcapped Polyynes Polyyne Synthesis Using Carbene—Carbenoid Rearrangements Tris (biphenyl‐4‐yl) silyl‐Endcapped Polyynes. Polyyne synthesis using carbene/carbenoid rearrangements

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Katalog der Deutschen Nationalbibliothek

Wesley Chalifoux

Chiral Teropyrenes: Synthesis, Structure, and Spectroscopic Studies

Chiral Teropyrenes: Synthesis, Structure, and Spectroscopic Studies

Dissymmetrical chiral peropyrenes: synthesis via iridium-catalyzed C–H activation/alkyne benzannulation and study of their properties

π‐Extended Helical Nanographenes: Synthesis and Photophysical Properties of Naphtho (1,2‐ a) pyrenes **

Synthesis and Structure of a Strained, Cyclic meta ‐Quaterphenylene Acetylene

Cover Feature: Synthesis and Structure of a Strained, Cyclic meta ‐Quaterphenylene Acetylene (Eur. J. Org. Chem. 28/2019)

Synthesis of Dihydroisobenzofuran Carboxaldehyde Derivatives by a Silver‐Catalyzed Sequential Protodesilylation/Cyclization/Oxidation Reaction

Synthesis, Structure, Photophysical Properties, and Photostability of Benzodipyrenes

Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes

Innentitelbild: Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes (Angew. Chem. 45/2018)

Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes

Inside Cover: Highly Regioselective Domino Benzannulation Reaction of Buta‐1,3‐diynes To Construct Irregular Nanographenes (Angew. Chem. Int. Ed. 45/2018)

Rapid π-Extension of Aromatics via Alkyne Benzannulations

Die Synthese von nichtplanaren, helikalen Graphen‐Nanobändern

The Synthesis of Non‐planar, Helically Coiled Graphene Nanoribbons

Synthesis of 2-Alkynyl-1,4-cyclohexadienes via a Diels–Alder Reaction of Conjugated 2,4-Diynones

Multicomponent Double Diels–Alder/Nazarov Tandem Cyclization of Symmetric Cross‐Conjugated Diynones to Generate (6‐5‐6) Tricyclic Products

Pyrenes, Peropyrenes, and Teropyrenes: Synthesis, Structures, and Photophysical Properties

Pyrenes, Peropyrenes, and Teropyrenes: Synthesis, Structures, and Photophysical Properties

ChemInform Abstract: Highly Regio‐ and Diastereoselective Formation of Tetrasubstituted (Z)‐1,2‐Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.

Photogenerated cumulenic structure of adamantyl endcapped linear carbon chains: An experimental and computational investigation based on infrared spectroscopy

ChemInform Abstract: Toward Carbyne: Synthesis and Stability of Really Long Polyynes

Polyine mit tert ‐Butyl‐Endgruppen: kristallographischer Nachweis einer reduzierten Bindungslängenalternanz †

tert ‐Butyl‐End‐Capped Polyynes: Crystallographic Evidence of Reduced Bond‐Length Alternation †

tert ‐Butyl‐End‐Capped Polyynes: Crystallographic Evidence of Reduced Bond‐Length Alternation †

Tris (biphenyl‐4‐yl) silyl‐Endcapped Polyynes

Polyyne Synthesis Using Carbene—Carbenoid Rearrangements

Tris (biphenyl‐4‐yl) silyl‐Endcapped Polyynes.

Polyyne synthesis using carbene/carbenoid rearrangements