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Publications 20102020

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Can the Ti(OiPr)4/nBuLi Combination of Reagents Function as a Catalyst for [2+2+2] Alkyne Cyclotrimerisation Reactions?

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G. Siemiaszko, Y. Six​

New J. Chem. 2018, 42, 20219−20226.

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1,3-Dipolar cycloadditions with azomethine ylide species generated from aminocyclopropanes

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A. Wolan, J. A. Kowalska-Six, H. Rajerison, M. Césario, M. Cordier, Y. Six​

Tetrahedron 2018, 74, 5248−5257.

(“Barton Centennial Symposium in Print” special issue)

2,3-Methanopyrrolidines: Synthesis and Ring-opening Transformations

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Y. Six

​in Targets in Heterocyclic Systems, O. A. Attanasi, P. Merino, D. Spinelli, Eds.;

Società Chimica Italiana: Roma (2017); Vol. 21, pp. 277−307.

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Synthesis of functionalised azepanes and piperidines from bicyclic halogenated aminocyclopropane derivatives

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C. Chen, P. Kattanguru, O. A. Tomashenko, R. Karpowicz, G. Siemiaszko,

A. Bhattacharya, V. Calasans, Y. Six

Org. Biomol. Chem. 2017, 15, 5364–5372.

(open access)

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Ring-opening, cycloaddition and rearrangement reactions of nitrogen-substituted cyclopropane derivatives

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V. A. Rassadin, Y. Six

Tetrahedron 2016, 72, 4701–4757.

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Access to New Endoperoxide Derivatives by Electrochemical Oxidation of Substituted 3-Azabicyclo[4.1.0]hept-4-enes

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F. Nuter, A. K. D. Dimé, C. Chen, L. Bounaadja, E. Mouray, I. Florent,

Y. Six, O. Buriez, A. Marinetti, A. Voituriez

Chem. Eur. J. 2015, 21, 5584–5593.

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Reductive Alkylation of Thioamides with Grignard Reagents in the Presence of Ti(OiPr)4: Insight and Extension

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F. Hermant, E. Urbańska, S. Seizilles de Mazancourt, T. Maubert, E. Nicolas, Y. Six

Organometallics 2014, 33, 5643–5653.

(“Catalytic and Organometallic Chemistry of Earth-Abundant Metals” special issue)

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Ti(OiPr)4/nBuLi: an attractive reagent system for [2+2+2] cyclotrimerisation reactions

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V. A. Rassadin, E. Nicolas, Y. Six

Chem. Commun. 2014, 50, 7666–7669.

(article highlighted by Synfacts: Synfacts 2014, 10, 968)

Ti-mediated intramolecular cyclopropanation of N-alkenyl thioamides: scope and mechanistic study

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F. Hermant, E. Nicolas, Y. Six

Tetrahedron 2014, 70, 3924–3930.

(article highlighted by Synfacts: Synfacts 2014, 10, 940)

Synthesis of polycyclic aminocyclobutane systems by the rearrangement of N-(ortho-vinylphenyl) 2-azabicyclo[3.1.0]hexane derivatives

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A. Wasilewska, B. A. Woźniak, G. Doridot, K. Piotrowska, N. Witkowska, P. Retailleau, Y. Six

Chem. Eur. J. 2013, 19, 11759−11567.

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Kulinkovich-type reactions of thioamides:
similar to those of carboxylic amides?

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E. Augustowska, A. Boiron, J. Deffit, Y. Six

Chem. Commun. 2012, 48, 5031–5033.

(article highlighted by Synfacts: Synfacts 2012, 8, 782)

Tactics for the asymmetric preparation of 2-azabicyclo
[3.1.0]hexane and 2-azabicyclo[4.1.0]heptane scaffolds

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A. Wolan, M. Soueidan, A. Chiaroni, P. Retailleau, S. Py, Y. Six

Tetrahedron Lett. 2011, 52, 2501–2504.

Aminocyclopropanes as precursors of endoperoxides with antimalarial activity

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C. Madelaine, O. Buriez, B. Crousse, I. Florent, P. Grellier, P. Retailleau, Y. Six

Org. Biomol. Chem. 2010, 8, 5591–5601.

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