LEI 11416 DE 2006 PDF

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Jumani, William Zuercher, Christopher D. Tandem One-Pot Synthesis of?

Harnessing Reversible Oxidative Addition: Rhodium-catalyzed asymmetric ring opening reactions of oxabicyclic alkenes: Exploring the mechanism of the Pd-catalyzed spirocyclization reaction: Marchese, Mark Lautens Org. Effects of halide ligands and protic additives on enantioselectivity and reactivity in rhodium-catalyzed asymmetric ring-opening reactions Lautens, M; Fagnou, K J.

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Lautens, M; Rovis, Ve Tetrahedron55 Use of Z -?

Industrial Chemical News4 Preparation of 2-substituted indole compound, useful for the synthesis of e. Palladium II catalyst systems for the addition of boronic acids to bicyclic alkenes: Rhodium-Catalyzed Enantioselective Nucleophilic Fluorination: Diastereoselective ring closing metathesis reactions: Lautens, M; Rovis, T Tetrahedron54 Rhodium-catalyzed asymmetric ring opening of oxabicyclic alkenes with sulfur nucleophiles Leong, P; Lautens, M J.

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Tsui, and Mark Lautens Angew. Newman and Mark Lautens J. Palladium catalyzed hydrostannation-cyclization of 1146. Rhodium-catalyzed asymmetric alcoholysis and aminolysis of oxabenzonorbornadiene: Science of Synthesis Volume 1pages. Base-induced ring opening of aza- and thiaoxa[3.

Rhodium-Catalyzed Enantioselective Reductive Arylation: Intramolecular cross-coupling of gem-dibromoolefins: Rebelo, Steffen Kress, Adam, A. An expedient enantioselective route to diaminotetralins: Friedman and Mark Lautens Synthesis48 Mild procedure for the catalytic bis stannylation of alkynes with hexaalkylditins Mancuso, J; Lautens, M Org.

Franke, and Mark Lautens Org.

Exploring the reactivity of dioxacyclic compounds as a route to polysubstituted decalins and fused polycycles Lautens, M; Fillion, E J. Preparing substituted azaindole compound, to e.

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A new route to fused aromatic compounds by using a palladium-catalyzed alkylation – Alkenylation sequence Lautens, M; Piguel, S Angew. A simple, cost-effective method for the regioselective deuteration of anilines Martins, A; Lautens, M Org. Department of Chemistry University of Toronto. Use of a sterically demanding Lewis acid to direct ring expansion of monoactivated methylenecyclopropanes Taillier, C; Bethuel, Y; Lautens, M Tetrahedron63 Chemodivergence in enantioselective desymmetrization of diazabicycles: Olson, Mark Lautens Org.

Lautens Research Group :: Publications

Newmanand Mark Lautens Org. Selective functionalization of 1,2-dihydronaphthalenols leads to a concise, stereoselective synthesis of sertraline. A cycloaddition-fragmentation-cyclization sequence to diquinanes and triquinanes Lautens, M; Blackwell, J Synthesis Synthesis of dihydronaphthalenes via Aryne Diels-Alder reactions: Bifunctional Reactivity of Cu-I: