Search Results - "Greaney, M. F."
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Corrigendum: The Benzyne Aza-Claisen Reaction
Published in Angewandte Chemie International Edition (08-10-2012)Get full text
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Reversible Michael addition of thiols as a new tool for dynamic combinatorial chemistry
Published in Chemical communications (Cambridge, England) (21-02-2005)“…The Michael addition of thiols to enones is reported as a new method for dynamic combinatorial library synthesis…”
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The First Total Synthesis of (±)-Ingenol
Published in Journal of the American Chemical Society (21-08-2002)“…The first total synthesis of (±)-ingenol has been achieved. The key features of the synthesis include the use of a highly diastereoselective Michael reaction…”
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A Paternò−Büchi Approach to the Synthesis of Merrilactone A
Published in Organic letters (01-09-2005)“…A six-step approach to the tetracyclic core of merrilactone A is described that uses an intramolecular Paternò−Büchi photoaddition to install the key oxetane…”
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Reagent-free Nazarov cyclisations
Published in Chemical communications (Cambridge, England) (07-02-2005)“…A new protocol for Nazarov cyclisation is described that involves simple heating of dienones in the absence of any external Lewis acid…”
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Studies on the oxidation and fluorination of α-phenylsulfanylacetamides using difluoroiodotoluene
Published in Tetrahedron letters (08-06-2000)“…α-Phenylsulfanylacetamides are fluorinated in the α-position when treated with difluoroiodotoluene (DFIT) in a fluoro-Pummerer reaction. For N-phenyl amides an…”
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Observations on the α-fluorination of α-phenylsulfanyl esters using difluoroiodotoluene
Published in Tetrahedron letters (08-06-2000)“…α-Phenylsulfanyl esters are fluorinated in the α-position when treated with the hypervalent iodine reagent difluoroiodotoluene. Excess reagent can lead to…”
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Studies on the additive fluoro-Pummerer reaction of phenylsulfanylated lactams with difluoroiodotoluene
Published in Tetrahedron letters (26-11-2001)“…Two fluorine atoms are effectively introduced to the 3- and 4-positions of sulfur-containing lactams through the action of the hypervalent iodoarene reagent…”
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