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A Practical in situ Generation of the Schwartz Reagent. Reduction of Tertiary Amides to Aldehydes and Hydrozirconation

Organic letters, 2014-01, Vol.16 (2), p.390-393

2014

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Beyond Directed ortho Metalation: Ru-Catalyzed CAr–O Activation/Cross-Coupling Reaction by Amide Chelation

Journal of the American Chemical Society, 2014-08, Vol.136 (32), p.11224-11227

2014

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N,N-Diethyl O-Carbamate: Directed Metalation Group and Orthogonal Suzuki−Miyaura Cross-Coupling Partner

Journal of the American Chemical Society, 2009-12, Vol.131 (49), p.17750-17752

2009

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Amide-Directed Ru-Catalyzed Hydrodemethoxylation of ortho‑Methoxy-Benzamides and -Naphthamides: A DoM Reaction Counterpart

Organic letters, 2018-05, Vol.20 (10), p.2826-2830

2018

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Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize

Angewandte Chemie (International ed.), 2012-05, Vol.51 (21), p.5062-5085

International ed. in English, 2012

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Directed aromatic functionalization

Beilstein journal of organic chemistry, 2011-09, Vol.7 (1), p.1215-1218

Snieckus, Victor

2011

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CH Activation by Amide Chelation Control: Ruthenium- Catalyzed Direct Synthesis of 2-Aryl-3-furanamides

Advanced synthesis & catalysis, 2014-05, Vol.356 (7), p.1527-1532

2014

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Identification of novel dynamin‐related protein 1 (Drp1) GTPase inhibitors: Therapeutic potential of Drpitor1 and Drpitor1a in cancer and cardiac ischemia‐reperfusion injury

The FASEB journal, 2020-01, Vol.34 (1), p.1447-1464

2020

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Beyond Thermodynamic Acidity: A Perspective on the Complex-Induced Proximity Effect (CIPE) in Deprotonation Reactions

Angewandte Chemie (International ed.), 2004-04, Vol.43 (17), p.2206-2225

2004

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Suzuki−Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies

Journal of the American Chemical Society, 2011-04, Vol.133 (16), p.6352-6363

2011

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Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics

Chemical reviews, 1990-09, Vol.90 (6), p.879-933

Snieckus, Victor

1990

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Combined Directed Remote Metalation−Transition Metal Catalyzed Cross Coupling Strategies: The Total Synthesis of the Aglycones of the Gilvocarcins V, M, and E and Arnottin I

Journal of organic chemistry, 2009-06, Vol.74 (11), p.4080-4093

2009

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Reductive Cleavage of Aryl O-Carbamates to Phenols by the Schwartz Reagent. Expedient Link to the Directed Ortho Metalation Strategy

Organic letters, 2013-08, Vol.15 (16), p.4102-4105

2013

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Sodium Methyl Carbonate as an Effective C1 Synthon. Synthesis of Carboxylic Acids, Benzophenones, and Unsymmetrical Ketones

Organic letters, 2019-06, Vol.21 (11), p.3882-3885

2019

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Copper-Catalyzed Cross-Coupling Interrupted by an Opportunistic Smiles Rearrangement: An Efficient Domino Approach to Dibenzoxazepinones

Angewandte Chemie (International ed.), 2012-03, Vol.51 (12), p.2925-2929

International ed. in English, 2012

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Directed ortho-Metalation–Cross-Coupling Strategies. One-Pot Suzuki Reaction to Biaryl and Heterobiaryl Sulfonamides

Organic letters, 2011-07, Vol.13 (14), p.3588-3591

2011

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Toxicity of hydroxylated alkyl-phenanthrenes to the early life stages of Japanese medaka ( Oryzias latipes)

Aquatic toxicology, 2012-01, Vol.106 (15), p.56-64

2012

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Quantitative structure–activity relationships for chronic toxicity of alkyl-chrysenes and alkyl-benz[a]anthracenes to Japanese medaka embryos (Oryzias latipes)

Aquatic toxicology, 2015-02, Vol.159, p.109-118

2015

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Beyond Directed ortho Metalation: Ru-Catalyzed C Ar –O Activation/Cross-Coupling Reaction by Amide Chelation

Journal of the American Chemical Society, 2014-08, Vol.136 (32), p.11224-11227

2014

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Directed ortho Metalation-Based Methodology. Halo-, Nitroso-, and Boro-Induced ipso-Desilylation. Link to an in situ Suzuki Reaction

Organic letters, 2005-06, Vol.7 (13), p.2523-2526

2005

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Combined Directed ortho and Remote Metalation−Suzuki Cross-Coupling Strategies. Efficient Synthesis of Heteroaryl-Fused Benzopyranones from Biaryl O-Carbamates

Journal of organic chemistry, 2009-06, Vol.74 (11), p.4094-4103

2009

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Studies of a ring-cleaving dioxygenase illuminate the role of cholesterol metabolism in the pathogenesis of Mycobacterium tuberculosis

PLoS pathogens, 2009-03, Vol.5 (3), p.e1000344-e1000344

2009

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Combined Directed Ortho and Remote Metalation−Cross-Coupling Strategies. General Method for Benzo[a]carbazoles and the Synthesis of an Unnamed Indolo[2,3-a]carbazole Alkaloid

Organic letters, 2004-07, Vol.6 (14), p.2293-2295

2004

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In Situ Anionic Shielding for Regioselective Metalation: Directed peri and Iterative Metalation Routes to Polyfunctionalized 7-Azaindoles

Angewandte Chemie (International ed.), 2012-03, Vol.51 (11), p.2722-2726

International ed. in English, 2012

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The directed ortho metalation—cross coupling symbiosis. Regioselective methodologies for biaryls and heterobiaryls. Deployment in aromatic and heteroaromatic natural product synthesis

Journal of Organometallic Chemistry, 2002-07, Vol.653 (1), p.150-160

2002

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A Practical in situ Generation of the Schwartz Reagent. Reduction of Tertiary Amides to Aldehydes and Hydrozirconation

Beyond Directed ortho Metalation: Ru-Catalyzed CAr–O Activation/Cross-Coupling Reaction by Amide Chelation

N,N-Diethyl O-Carbamate: Directed Metalation Group and Orthogonal Suzuki−Miyaura Cross-Coupling Partner

Amide-Directed Ru-Catalyzed Hydrodemethoxylation of ortho‑Methoxy-Benzamides and -Naphthamides: A DoM Reaction Counterpart

Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize

Directed aromatic functionalization

CH Activation by Amide Chelation Control: Ruthenium- Catalyzed Direct Synthesis of 2-Aryl-3-furanamides

Identification of novel dynamin‐related protein 1 (Drp1) GTPase inhibitors: Therapeutic potential of Drpitor1 and Drpitor1a in cancer and cardiac ischemia‐reperfusion injury

Beyond Thermodynamic Acidity: A Perspective on the Complex-Induced Proximity Effect (CIPE) in Deprotonation Reactions

Suzuki−Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies

Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics

Combined Directed Remote Metalation−Transition Metal Catalyzed Cross Coupling Strategies: The Total Synthesis of the Aglycones of the Gilvocarcins V, M, and E and Arnottin I

Reductive Cleavage of Aryl O-Carbamates to Phenols by the Schwartz Reagent. Expedient Link to the Directed Ortho Metalation Strategy

Sodium Methyl Carbonate as an Effective C1 Synthon. Synthesis of Carboxylic Acids, Benzophenones, and Unsymmetrical Ketones

Copper-Catalyzed Cross-Coupling Interrupted by an Opportunistic Smiles Rearrangement: An Efficient Domino Approach to Dibenzoxazepinones

Directed ortho-Metalation–Cross-Coupling Strategies. One-Pot Suzuki Reaction to Biaryl and Heterobiaryl Sulfonamides

Toxicity of hydroxylated alkyl-phenanthrenes to the early life stages of Japanese medaka ( Oryzias latipes)

Quantitative structure–activity relationships for chronic toxicity of alkyl-chrysenes and alkyl-benz[a]anthracenes to Japanese medaka embryos (Oryzias latipes)

Beyond Directed ortho Metalation: Ru-Catalyzed C Ar –O Activation/Cross-Coupling Reaction by Amide Chelation

Directed ortho Metalation-Based Methodology. Halo-, Nitroso-, and Boro-Induced ipso-Desilylation. Link to an in situ Suzuki Reaction

Combined Directed ortho and Remote Metalation−Suzuki Cross-Coupling Strategies. Efficient Synthesis of Heteroaryl-Fused Benzopyranones from Biaryl O-Carbamates

Studies of a ring-cleaving dioxygenase illuminate the role of cholesterol metabolism in the pathogenesis of Mycobacterium tuberculosis

Combined Directed Ortho and Remote Metalation−Cross-Coupling Strategies. General Method for Benzo[a]carbazoles and the Synthesis of an Unnamed Indolo[2,3-a]carbazole Alkaloid

In Situ Anionic Shielding for Regioselective Metalation: Directed peri and Iterative Metalation Routes to Polyfunctionalized 7-Azaindoles

The directed ortho metalation—cross coupling symbiosis. Regioselective methodologies for biaryls and heterobiaryls. Deployment in aromatic and heteroaromatic natural product synthesis

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