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Carbonylative Cross-Coupling of ortho -Disubstituted Aryl Iodides. Convenient Synthesis of Sterically Hindered Aryl Ketones

✍ Scribed by O’Keefe, B. Michael; Simmons, Nicholas; Martin, Stephen F.

Book ID
127154778
Publisher
American Chemical Society
Year
2008
Tongue
English
Weight
110 KB
Volume
10
Category
Article
ISSN
1523-7060

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📜 SIMILAR VOLUMES

ChemInform Abstract: Carbonylative Cross
ChemInform Abstract: Carbonylative Cross-Coupling of ortho-Disubstituted Aryl Iodides. Convenient Synthesis of Sterically Hindered Aryl Ketones.
✍ B. Michael O'Keefe; Nicholas Simmons; Stephen F. Martin 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Facile Access to St
ChemInform Abstract: Facile Access to Sterically Hindered Aryl Ketones via Carbonylative Cross-Coupling: Application to the Total Synthesis of Luteolin.
✍ B. Michael O'Keefe; Nicholas Simmons; Stephen F. Martin 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 56 KB 👁 2 views

## Abstract Novel variants of the carbonylative Suzuki and Negishi cross‐coupling reaction of sterically hindered aryl iodides are developed using commercially available PEPPSI‐IPr as the catalyst.