A palladium-catalyzed cyclization-carbonylation-coupling reaction between aryl halides and γ-Hydroxyallenes to form aryl (tetrahydrofuran-2-yl)vinyl ketones-Reference-Cited by-同舟云学术

A palladium-catalyzed cyclization-carbonylation-coupling reaction between aryl halides and γ-Hydroxyallenes to form aryl (tetrahydrofuran-2-yl)vinyl ketones

Published:1995-05 Issue:22 Volume:36 Page:3805-3808
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Walkup Robert D.,Guan Lufeng,Kim Young Soo,Kim Sang Woong

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. Palladium-catalyzed reaction of vinyl triflates and vinyl/aryl halides with 4-alkynoic acids: regio- and stereoselective synthesis of (E)-.delta.-vinyl/aryl-.gamma.-methylene-.gamma.-butyrolactones

2. Intramolecular oxypalladation and cross-coupling of acetylenic alkoxides

3. Intramolecular aminopalladation and cross coupling of acetylenic amines

4. Metal Ion-Mediated Heteroatom Cyclisations. Application of Aryl/Alkenyl Palladium(II)-Based Electrophilic Triggers

5. Cyclizations of γ-Hydroxyallenes Mediated by Organopalladium Halides: A Convergent Synthetic Route to Substituted 5-Alkenyl-2-furanones and 2-Alkenyltetrahydrofurans

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