✦ LIBER ✦

Palladium-Catalyzed Synthesis of N -Vinyl Pyrroles and Indoles

✍ Scribed by Movassaghi, Mohammad; Ondrus, Alison E.

Book ID: 118034557
Publisher: American Chemical Society
Year: 2005
Tongue: English
Weight: 129 KB
Volume: 70
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo051450i

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Palladium-Catalyzed Synthesis of N-Vinyl

Palladium-Catalyzed Synthesis of N-Vinyl Pyrroles and Indoles.

✍ Mohammad Movassaghi; Alison E. Ondrus 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 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, please click on HTML or PDF.

Palladium-catalyzed synthesis of pyrrole

Palladium-catalyzed synthesis of pyrroles

✍ Kiitiro Utimoto; Hiroshi Miwa; Hitosi Nozaki 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 115 KB

Pyrrole derivatives are prepared in high yields by the catalytic action of a Pd(II) salt on l-amino-3-alkyn-2-01s which are obtained from conjugate ynones.

Palladium-catalyzed synthesis of fused i

Palladium-catalyzed synthesis of fused indoles

✍ Björn C. Söderberg; Stacey R. Rector; Shannon N. O'Neil 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 235 KB

Phosphine-Free Palladium-Catalyzed C—H B

Phosphine-Free Palladium-Catalyzed C—H Bond Arylation of Free (N—H)-Indoles and Pyrroles.

✍ Xiang Wang; Denis V. Gribkov; Dalibor Sames 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

Phosphine-Free Palladium-Catalyzed C−H B

Phosphine-Free Palladium-Catalyzed C−H Bond Arylation of Free (N−H)-Indoles and Pyrroles

✍ Wang, Xiang; Gribkov, Denis V.; Sames, Dalibor 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 202 KB

Synthesis of N-vinyl substituted indoles

Synthesis of N-vinyl substituted indoles and their acid-catalyzed behavior

✍ Hao Li; Nawong Boonnak; Albert Padwa 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 328 KB

A mild cross-coupling reaction has been used to access several N-vinyl substituted indoles. When treated with acid, these unique enamines produce novel dimeric and trimeric products derived from a preferred protonation reaction at the enamine p-bond.