✦ LIBER ✦

Palladium-Catalyzed Heck and Carbonylation Reactions of a Dinaphthaleneiodonium Salt Forming Functionalized 2-Iodo-1,1′-binaphthyls

✍ Scribed by Asato Kina; Hiroyuki Miki; Yong-Hwan Cho; Tamio Hayashi

Publisher: John Wiley and Sons
Year: 2004
Tongue: English
Weight: 152 KB
Volume: 346
Category: Article
ISSN: 1615-4150
DOI: 10.1002/adsc.200404202

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Palladium-Catalyzed

ChemInform Abstract: Palladium-Catalyzed Reactions. Part 2. Suzuki Coupling of Chiral 1,1′-Binaphthyl Systems — New Synthetic Routes to Functionalize the 2- and 2,2′-Positions.

✍ B. SCHILLING; D. E. KAUFMANN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

A General Approach to Selective Function

A General Approach to Selective Functionalization of 1,2,4-Triazines Using Organometallics in Palladium-Catalyzed Cross-Coupling and Addition Reactions.

✍ France-Aimee Alphonse; Franck Suzenet; Anne Keromnes; Bruno Lebret; Gerald Guill 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

A new approach to the synthesis of funct

A new approach to the synthesis of functionalized pyrido[2,3-b]indoles by way of a palladium-catalyzed ring closing reaction between the N-1 and C-9a positions

✍ Ahmed Abouabdellah; Robert H. Dodd 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 238 KB

The enolate of 4-N-(tert-butyloxycarbonyl)aminobutyro-7-lacto~e 9 reacted with 2-bromo-1methylindole-3-carboxaldehyde it, the presence of stannic chloride to give the product of aldol condensation 16. Deprotection and dehydration of the latter with trifluoroacetic' acid and dimethyl sulfide followed

ChemInform Abstract: A New Approach to t

ChemInform Abstract: A New Approach to the Synthesis of Functionalized Pyrido[2,3-b]indoles by Way of a Palladium-Catalyzed Ring Closing Reaction Between the N-1 and C-9a Positions.

✍ A. ABOUABDELLAH; R. H. DODD 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views