Stereoselective Synthesis of Stannyl Enones via Palladium-Catalyzed and Free Radical Hydrostannation of Alkynyl Ketones with Trineophyltin Hydride-Reference-Cited by-同舟云学术

Stereoselective Synthesis of Stannyl Enones via Palladium-Catalyzed and Free Radical Hydrostannation of Alkynyl Ketones with Trineophyltin Hydride

Published:2003-12-01 Issue:26 Volume:68 Page:10087-10091
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dodero Verónica I.¹,Koll Liliana C.¹,Belén Faraoni M.¹,Mitchell Terence N.¹,Podestá Julio C.¹

Affiliation:

1. Departamento de Química, Universidad Nacional del Sur, Avenida Alem 1253, 8000 Bahía Blanca, and CONICET Buenos Aires, Argentina, and Fachbereich Chemie Universität Dortmund, D-44221 Dortmund, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035396m

Reference22 articles.

1. Total Synthesis of the Enantiomer of the Antiviral Marine Natural Product Hennoxazole A

2. Radical Cyclization of Polyenes Initiated by Attack of Trialkyltin or Germanium Radical on an Ynone

3. An Enantioselective Synthetic Route to Atractyligenin Using the Oxazaborolidine-Catalyzed Reduction of β-Silyl- or β-Stannyl-Substituted α,β-Enones as a Key Step

4. Tin-directed nazarov cyclizations: A versatile route to cyclopentenoids

5. .beta.-Stannyl enones as radical traps: a very direct route to PGF2.alpha.

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