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Victor Snieckus

Researcher at Queen's University

Publications -  999
Citations -  11201

Victor Snieckus is an academic researcher from Queen's University. The author has contributed to research in topics: Directed ortho metalation & Metalation. The author has an hindex of 48, co-authored 999 publications receiving 10225 citations. Previous affiliations of Victor Snieckus include University of British Columbia & University of Münster.

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Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize

Carin C. C. Johansson Seechurn, +3 more
- 21 May 2012 - 
TL;DR: This Review attempts to trace the historical origin of these powerful reactions, and outline the developments from the seminal discoveries leading to their eminent position as appreciated and applied today.
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Beyond Thermodynamic Acidity: A Perspective on the Complex‐Induced Proximity Effect (CIPE) in Deprotonation Reactions

Marna C. Whisler, +3 more
- 19 Apr 2004 - 
TL;DR: The consequences of complexation of organolithium bases to functional groups of the substrates before the proton-transfer step are discussed and of particular interest is the functionalization of positions that are remote from the coordination group.
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Palladiumkatalysierte Kreuzkupplungen: eine historische Perspektive im Kontext der Nobel-Preise 2010

Carin C. C. Johansson Seechurn, +3 more
- 21 May 2012 - 
TL;DR: In 2010, Heck, Ei-ichi Negishi and Akira Suzuki were aufgenommen in den illustren Kreis der Chemie-Nobelpreistrager (C-C-Bindungsbildung).
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Directed lithiation of aromatic tertiary amides: an evolving synthetic methodology for polysubstituted aromatics

Peter Beak, +1 more
- 01 Oct 1982 - 
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Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.

Kyle W. Quasdorf, +9 more
- 27 Apr 2011 - 
TL;DR: The first Suzuki-Miyaura cross-coupling reactions of the synthetically versatile aryl O-carbamate and O-sulfamate groups are described and several synthetic applications are presented to showcase the utility of the methodology in the synthesis of polysubstituted aromatic compounds of natural product and bioactive molecule interest.