✦ LIBER ✦

ChemInform Abstract: Silylcupration and Copper-Catalyzed Carbomagnesiation of Ynamides: Application to Aza-Claisen Rearrangement.

✍ Scribed by Hiroto Yasui; Hideki Yorimitsu; Koichiro Oshima

Book ID: 102019537
Publisher: John Wiley and Sons
Year: 2008
Weight: 48 KB
Volume: 39
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200831052

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Aza-Pinacol Rearran

ChemInform Abstract: Aza-Pinacol Rearrangement: Acid-Catalyzed Rearrangement of Aziridines to Imines.

✍ Yoshiaki Sugihara; Shinya Iimura; Juzo Nakayama 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

ChemInform Abstract: Copper-Catalyzed Hi

ChemInform Abstract: Copper-Catalyzed Highly Regioselective Silylcupration of Terminal Alkynes to Form α-Vinylsilanes.

✍ Peng Wang; Xue-Liang Yeo; Teck-Peng Loh 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 29 KB

ChemInform Abstract: A New Palladium(II)

ChemInform Abstract: A New Palladium(II)-Catalyzed [3,3] Aza-Claisen Rearrangement of 3-Allyloxy-5-aryl-1,2,4-oxadiazoles.

✍ Gianfranco Fontana; Antonio Palumbo Piccionello 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 30 KB

ChemInform Abstract: Optimization of the

ChemInform Abstract: Optimization of the Microwave-Assisted Orthoester Claisen Rearrangement: Application to Monoterpenols.

✍ Florence Mehl; Isabelle Bombarda; Carine Franklin; Emile M. Gaydou 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 22 KB 👁 2 views

ChemInform Abstract: Application of the

ChemInform Abstract: Application of the Chelate Enolate Claisen Rearrangement to the Modification of Dipeptides.

✍ Uli Kazmaier; Sabine Maier 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

ChemInform Abstract: Synthetic and Mecha

ChemInform Abstract: Synthetic and Mechanistic Studies of the Aza-Retro-Claisen Rearrangement. A Facile Route to Medium Ring Nitrogen Heterocycles.

✍ Robert K. Jr. Boeckman; Nathan E. Genung; Ke Chen; Todd R. Ryder 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 60 KB 👁 2 views

## Abstract Heating of oxepines and oxacenes of type (I) and (IV) as well as cyclobutanecarboxaldehydes like (VII) with Staudinger reagents is found to provide an efficient approach to medium ring nitrogen heterocycles.