V
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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Journal ArticleDOI
Regioselective Functionalization of 7-Azaindole by Controlled Annular Isomerism: The Directed Metalation-Group Dance.
Michael E. Dalziel,Jignesh J. Patel,Meagan K. Kaye,Jennifer L. Cosman,Matthew O. Kitching,Victor Snieckus +5 more
TL;DR: The regioselective functionalization of 7-azaindole by controlled annular isomerism employing a directed metalation-group migration is reported and a late-stage deuteration of an antipsychotic drug is described.
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A new convenient synthesis of bifunctional chelating agent 1-(4-aminobenzyl)-1,4,8,11-tetraazacyclotetradecane-N′,N″,N‴-triacetic acid [1-(H2NBn-TETA)]
TL;DR: In this paper, a boron-protection strategy was proposed for the bifunctional chelating agent 1-(4-aminobenzyl)-1,4,8,11-tetraazacyclotetradecane-N′-,N″-,N''-,N´-triacetic acid (4) via a bore-protection mechanism.
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Ferroelectric liquid crystals with fluoro‐ and aza‐fluorenone cores: the effect of stereo‐polar coupling
TL;DR: The chiral fluorenone mesogens (R) as discussed by the authors were synthesized usin 1998, and were used to synthesize the following mesogens: 1.1.fluoro, 2.2.octyloxy, 7.4.undecyloxybenzoyloxy, 3.3.azafluoren, and 9.9.one.
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Metal-Free Synthesis of Dibenzoxazepinones via a One-Pot SNAr and Smiles Rearrangement Process: Orthogonality with Copper-Catalyzed Cyclizations
Timothy E. Hurst,Matthew O. Kitching,Lívia C. R. M. da Frota,Lívia C. R. M. da Frota,Keller G. Guimarães,Keller G. Guimarães,Michael E. Dalziel,Victor Snieckus +7 more
TL;DR: In this paper, a transition-metal-free synthesis of substituted dibenzoxazepinones using a convergent domino SNAr-Smiles rearrangement-SNAr process was reported.
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A Practical in situ Generation of the Schwartz Reagent. Reduction of Tertiary Amides to Aldehydes and Hydrozirconation.
Yigang Zhao,Victor Snieckus +1 more
TL;DR: In this article, a new protocol (Cp2ZrCl2/LiAlH(OBu-t)3) is described for the generation of Schwartz reagent which provides a convenient method for the amide to aldehyde reduction and the regioselective hydrozirconation-iodination of alkynes and alkenes.