Synthesis of 2H-1-Benzopyrans via Palladacycles with a Metal-Bonded Stereogenic Carbon
- 18 September 2002
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 4 (21) , 3679-3681
- https://doi.org/10.1021/ol0201456
Abstract
Stable oxapalladacycles have been prepared and converted into a series of highly functionalized 2H-1-benzopyrans via regioselective insertion of activated alkynes.Keywords
This publication has 8 references indexed in Scilit:
- A Novel Palladium-Catalyzed Synthesis of Phenanthrenes from ortho-Substituted Aryl Iodides and Diphenyl- or AlkylphenylacetylenesOrganic Letters, 2001
- Synthesis of 9-Alkylidene-9H-fluorenes by a Novel, Palladium-Catalyzed Cascade Reaction of Aryl Halides and 1-Aryl-1-alkynesThe Journal of Organic Chemistry, 2001
- An Exploratory Study of Regiocontrol in the Heck Type Reaction. Influence of Solvent Polarity and Bisphosphine LigandsOrganometallics, 1999
- Palladium-Catalyzed Coupling of Naphthoquinone Triflates with Stannanes. Unprecedented Nucleophilic Aromatic Substitution on a Hydroxynaphthoquinone TriflateThe Journal of Organic Chemistry, 1997
- A Complex Catalytic Cycle Leading to a Regioselective Synthesis of o,o′‐Disubstituted VinylarenesAngewandte Chemie International Edition in English, 1997
- Synthesis and structural studies of phenyl(iodo)- and methyl(phenyl)palladium(II) complexes of bidentate nitrogen donor ligandsJournal of Organometallic Chemistry, 1994
- Preparation and reactions of bis(triphenylphosphine)palladium(0)Journal of Organometallic Chemistry, 1989
- New preparation of coumaransThe Journal of Organic Chemistry, 1970