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Reductive Hydroxymethylation of 4‐Heteroarylpyridines

Chemistry : a European journal, 2020-02, Vol.26 (9), p.1963-1967

2020

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Hypervalent iodine initiated intramolecular alkene dimerisation: a stereodivergent entry to cyclobutanes

Chemical communications (Cambridge, England), 2019, Vol.55 (69), p.1316-1319

2019

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Orthogonally Protected 1,2-Diols from Electron-Rich Alkenes Using Metal-Free Olefin syn-Dihydroxylation

Organic letters, 2016-11, Vol.18 (22), p.5880-5883

2016

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Recent Developments in Methodology for the Direct Oxyamination of Olefins

Chemistry : a European journal, 2011-01, Vol.17 (1), p.58-76

2011

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Ring-Closing Metathesis: Novel Routes to Aromatic Heterocycles

Chemistry : a European journal, 2008-06, Vol.14 (19), p.5716-5726

2008

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expedient route to substituted furans via olefin cross-metathesis

Proceedings of the National Academy of Sciences - PNAS, 2010-02, Vol.107 (8), p.3373-3376

2010

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Asymmetric Total Synthesis of (−)-(3R)‑Inthomycin C

Organic letters, 2018-06, Vol.20 (12), p.3583-3586

2018

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OBO-Protected Pyruvates as Reagents for the Synthesis of Functionalized Heteroaromatic Compounds

Organic letters, 2018-07, Vol.20 (13), p.4048-4051

2018

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Direct preparation of thiazoles, imidazoles, imidazopyridines and thiazolidines from alkenes

Organic & biomolecular chemistry, 2012-02, Vol.10 (5), p.1093-1101

2012

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Modular Isoquinoline Synthesis Using Catalytic Enolate Arylation and in Situ Functionalization

Organic letters, 2013-12, Vol.15 (24), p.6190-6193

2013

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Heteroaromatic Synthesis via Olefin Cross-Metathesis: Entry to Polysubstituted Pyridines

Organic letters, 2011-03, Vol.13 (5), p.1036-1039

2011

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Olefin cross-metathesis for the synthesis of heteroaromatic compounds

Organic & biomolecular chemistry, 2012-02, Vol.1 (7), p.1322-1328

2012

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Pyruvate Enolate Arylation and Alkylation: OBO Ester Protected Pyruvates as Useful Reagents in Organic Synthesis

Organic letters, 2017-10, Vol.19 (19), p.5248-5251

2017

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Total Synthesis of the Antitumor Antibiotic (±)-Streptonigrin: First- and Second-Generation Routes for de Novo Pyridine Formation Using Ring-Closing Metathesis

Journal of organic chemistry, 2013-12, Vol.78 (24), p.12338-12350

2013

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Palladium-catalyzed enolate arylation as a key C-C bond-forming reaction for the synthesis of isoquinolines

Organic & biomolecular chemistry, 2016-01, Vol.14 (3), p.1065-1090

2016

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A Metathesis-Based Approach to the Synthesis of 2-Pyridones and Pyridines

Organic letters, 2008-01, Vol.10 (2), p.285-288

2008

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Synthesis of lamellarin alkaloids using orthoester-masked α-keto acids

Chemical science (Cambridge), 2019-04, Vol.10 (15), p.4334-4338

2019

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Tethered Aminohydroxylation Reaction and Its Application to Total Synthesis

European Journal of Organic Chemistry, 2012-02, Vol.2012 (4), p.655-663

2012

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Asymmetric Synthesis of the Fully Elaborated Pyrrolidinone Core of Oxazolomycin A

Organic letters, 2012-11, Vol.14 (21), p.5460-5463

2012

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N-Sulfonyloxy Carbamates as Reoxidants for the Tethered Aminohydroxylation Reaction

Journal of the American Chemical Society, 2006-03, Vol.128 (8), p.2514-2515

2006

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Regioselective Nucleophilic Addition to Pyridinium Salts: A New Route to Substituted Dihydropyridones

Organic letters, 2009-12, Vol.11 (23), p.5562-5565

2009

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A Noncarbohydrate Based Approach to Polyhydroxylated Pyrrolidizines: Total Syntheses of the Natural Products Hyacinthacine A1 and 1-Epiaustraline

Journal of organic chemistry, 2005-09, Vol.70 (18), p.7297-7304

2005

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Tethered Aminohydroxylation: Dramatic Improvements to the Process

Organic letters, 2007-04, Vol.9 (9), p.1725-1728

2007

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Directed Dihydroxylation of Cyclic Allylic Alcohols and Trichloroacetamides Using OsO4/TMEDA

Journal of organic chemistry, 2002-11, Vol.67 (23), p.7946-7956

2002

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Rhodium catalysed C-3/5 methylation of pyridines using temporary dearomatisation

Chemical science (Cambridge), 2020-08, Vol.11 (32), p.8595-8599

2020

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Reductive Hydroxymethylation of 4‐Heteroarylpyridines

Hypervalent iodine initiated intramolecular alkene dimerisation: a stereodivergent entry to cyclobutanes

Orthogonally Protected 1,2-Diols from Electron-Rich Alkenes Using Metal-Free Olefin syn-Dihydroxylation

Recent Developments in Methodology for the Direct Oxyamination of Olefins

Ring-Closing Metathesis: Novel Routes to Aromatic Heterocycles

expedient route to substituted furans via olefin cross-metathesis

Asymmetric Total Synthesis of (−)-(3R)‑Inthomycin C

OBO-Protected Pyruvates as Reagents for the Synthesis of Functionalized Heteroaromatic Compounds

Direct preparation of thiazoles, imidazoles, imidazopyridines and thiazolidines from alkenes

Modular Isoquinoline Synthesis Using Catalytic Enolate Arylation and in Situ Functionalization

Heteroaromatic Synthesis via Olefin Cross-Metathesis: Entry to Polysubstituted Pyridines

Olefin cross-metathesis for the synthesis of heteroaromatic compounds

Pyruvate Enolate Arylation and Alkylation: OBO Ester Protected Pyruvates as Useful Reagents in Organic Synthesis

Total Synthesis of the Antitumor Antibiotic (±)-Streptonigrin: First- and Second-Generation Routes for de Novo Pyridine Formation Using Ring-Closing Metathesis

Palladium-catalyzed enolate arylation as a key C-C bond-forming reaction for the synthesis of isoquinolines

A Metathesis-Based Approach to the Synthesis of 2-Pyridones and Pyridines

Synthesis of lamellarin alkaloids using orthoester-masked α-keto acids

Tethered Aminohydroxylation Reaction and Its Application to Total Synthesis

Asymmetric Synthesis of the Fully Elaborated Pyrrolidinone Core of Oxazolomycin A

N-Sulfonyloxy Carbamates as Reoxidants for the Tethered Aminohydroxylation Reaction

Regioselective Nucleophilic Addition to Pyridinium Salts: A New Route to Substituted Dihydropyridones

A Noncarbohydrate Based Approach to Polyhydroxylated Pyrrolidizines: Total Syntheses of the Natural Products Hyacinthacine A1 and 1-Epiaustraline

Tethered Aminohydroxylation: Dramatic Improvements to the Process

Directed Dihydroxylation of Cyclic Allylic Alcohols and Trichloroacetamides Using OsO4/TMEDA

Rhodium catalysed C-3/5 methylation of pyridines using temporary dearomatisation

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