ChemInform Abstract: Single-Flask Multicomponent Palladium-Catalyzed α,γ-Coupling of Ketone Enolates: Facile Preparation of Complex Carbon Scaffolds.

10.1002/chin.201605065 ◽

2016 ◽

Vol 47 (5) ◽

pp. no-no

Author(s):

Michael Grigalunas ◽

Per-Ola Norrby ◽

Olaf Wiest ◽

Paul Helquist

Keyword(s):

Ketone Enolates ◽

Palladium Catalyzed ◽

Facile Preparation ◽

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Single-Flask Multicomponent Palladium-Catalyzed α,γ-Coupling of Ketone Enolates: Facile Preparation of Complex Carbon Scaffolds

Angewandte Chemie ◽

10.1002/ange.201505895 ◽

2015 ◽

Vol 127 (40) ◽

pp. 11988-11991 ◽

Author(s):

Michael Grigalunas ◽

Per-Ola Norrby ◽

Olaf Wiest ◽

Paul Helquist

Keyword(s):

Ketone Enolates ◽

Palladium Catalyzed ◽

Facile Preparation ◽

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Single-Flask Multicomponent Palladium-Catalyzed α,γ-Coupling of Ketone Enolates: Facile Preparation of Complex Carbon Scaffolds

Angewandte Chemie International Edition ◽

10.1002/anie.201505895 ◽

2015 ◽

Vol 54 (40) ◽

pp. 11822-11825 ◽

Author(s):

Michael Grigalunas ◽

Per-Ola Norrby ◽

Olaf Wiest ◽

Paul Helquist

Keyword(s):

Ketone Enolates ◽

Palladium Catalyzed ◽

Facile Preparation ◽

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ChemInform Abstract: Facile Preparation of Indoles and 1,2-Benzothiazine 1,1-Dioxides: Nucleophilic Addition of Sulfonamides to Bromoacetylenes and Subsequent Palladium-Catalyzed Cyclization.

10.1002/chin.201245130 ◽

2012 ◽

Vol 43 (45) ◽

pp. no-no

Author(s):

Masahito Yamagishi ◽

Ken Nishigai ◽

Azusa Ishii ◽

Takeshi Hata ◽

Hirokazu Urabe

Keyword(s):

Nucleophilic Addition ◽

Palladium Catalyzed ◽

Facile Preparation

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A facile preparation of 1-perflouroalkylalkenes and alkynes. Palladium catalyzed reaction of perfluoroalkyl iodides with organotin compounds

Tetrahedron Letters ◽

10.1016/s0040-4039(01)81073-x ◽

1987 ◽

Vol 28 (47) ◽

pp. 5857-5860 ◽

Author(s):

Seijiro Matsubara ◽

Makoto Mitani ◽

Kiitiro Utimoto

Keyword(s):

Organotin Compounds ◽

Palladium Catalyzed ◽

Facile Preparation

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The palladium-catalyzed michael addition reaction of the ketone enolates generated by the decarboxylation of allyl β-keto carboxylates under neutral conditions

Tetrahedron Letters ◽

10.1016/s0040-4039(01)80520-7 ◽

1989 ◽

Vol 30 (36) ◽

pp. 4829-4832 ◽

Author(s):

Jnuzo Nokami ◽

Hisayuki Watanabe ◽

Tadakatsu Mandai ◽

Mikio Kawada ◽

Jiro Tsuji

Keyword(s):

Michael Addition ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Ketone Enolates ◽

Palladium Catalyzed ◽

Neutral Conditions

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Palladium-Catalyzed Alkenylation of Ketone Enolates under Mild Conditions

Organic Letters ◽

10.1021/ol5017965 ◽

2014 ◽

Vol 16 (15) ◽

pp. 3970-3973 ◽

Author(s):

Michael Grigalunas ◽

Tobias Ankner ◽

Per-Ola Norrby ◽

Olaf Wiest ◽

Paul Helquist

Keyword(s):

Mild Conditions ◽

Ketone Enolates ◽

Palladium Catalyzed

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Palladium-Catalyzed Intramolecular Coupling of Aryl Halides and Ketone Enolates: Synthesis of Hexahydro-2,6-methano-1-benzazocines

Advanced Synthesis & Catalysis ◽

10.1002/1615-4169(200107)343:5<439::aid-adsc439>3.0.co;2-g ◽

2001 ◽

Vol 343 (5) ◽

pp. 439-442 ◽

Author(s):

Daniel Solé ◽

Lluís Vallverdú ◽

Josep Bonjoch

Keyword(s):

Aryl Halides ◽

Ketone Enolates ◽

Palladium Catalyzed

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Unusual Selectivity of Unprotected Aziridines in Palladium-Catalyzed Allylic Amination Enables Facile Preparation of Branched Aziridines

Journal of the American Chemical Society ◽

10.1021/ja049242f ◽

2004 ◽

Vol 126 (16) ◽

pp. 5086-5087 ◽

Author(s):

Iain D. G. Watson ◽

Sarah A. Styler ◽

Andrei K. Yudin

Keyword(s):

Allylic Amination ◽

Palladium Catalyzed ◽

Facile Preparation

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ChemInform Abstract: Efficient Trapping of Ketone Enolates with Acrylate and β-Sulfonylacrylate Thioesters, β-Sulfonyl-, β-Sulfinyl- and β-Chloro-vinyl Ketones; Facile Preparation of a Hydrindanone, cis-Dimethyloctalone, and Unsaturated 1,5-Dicarbonyl Com

10.1002/chin.199050110 ◽

1990 ◽

Vol 21 (50) ◽

Author(s):

R. J. DANCER ◽

R. K. HAYNES ◽

W. A. LOUGHLIN ◽

S. C. VONWILLER

Keyword(s):

Ketone Enolates ◽

Facile Preparation

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A facile preparation of 4-aryl-3-[(tert-butyldimethylsilyl)oxymethyl]furans

Canadian Journal of Chemistry ◽

10.1139/v91-197 ◽

1991 ◽

Vol 69 (8) ◽

pp. 1326-1330 ◽

Author(s):

Brian A. Keay ◽

Jean-Louis J. Bontront

Keyword(s):

Key Words ◽

Coupling Reaction ◽

Aryl Bromides ◽

Palladium Catalyzed ◽

Facile Preparation

A series of aryl bromides undergo a palladium-catalyzed coupling reaction with 3-[(tert-butyldimethylsilyl)oxymethyl]-4-(tri-n-butylstannyl)furan to provide 4-aryl-3-[(tert-butyldimethylsilyl)oxymethyl]furans in moderate to good yields. Key words: palladium, cross-couplings, stannanes, 3,4-disubstituted furans.

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