✦ LIBER ✦

Facile Access to Key Reactive Intermediates in the Pd/PR3-Catalyzed Telomerization of 1,3-Butadiene

✍ Scribed by Peter J. C. Hausoul; Dr. Andrei N. Parvulescu; Dr. Martin Lutz; Prof. Dr. Anthony L. Spek; Dr. Pieter C. A. Bruijnincx; Prof. Dr. Bert M. Weckhuysen; Prof. Dr. Robertus J. M. Klein Gebbink

Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 400 KB
Volume: 122
Category: Article
ISSN: 0044-8249
DOI: 10.1002/ange.201003090

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Facile Access to Key Reactive Intermedia

Facile Access to Key Reactive Intermediates in the Pd/PR3-Catalyzed Telomerization of 1,3-Butadiene

✍ Peter J. C. Hausoul; Dr. Andrei N. Parvulescu; Dr. Martin Lutz; Prof. Dr. Anthon 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 419 KB 👁 2 views

ChemInform Abstract: Access to a Novel C

ChemInform Abstract: Access to a Novel Class of Tetracyclic 1,4-Benzodiazepin-5-ones Starting from α-Amino Acids by Pd-Catalyzed Amination/1,3-Dipolar Cycloaddition as the Key Steps.

✍ Luca Basolo; Egle M. Beccalli; Elena Borsini; Gianluigi Broggini; Maisaa Khansaa 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 2 views

ChemInform Abstract: Effects of Substitu

ChemInform Abstract: Effects of Substituents in the β-Position of 1,3-Dicarbonyl Compounds in Bromodimethylsulfonium Bromide Catalyzed Multicomponent Reactions: A Facile Access to Functionalized Piperidines.

✍ Abu T. Khan; Tasneem Parvin; Lokman H. Choudhury 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 42 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Isolation of Methyl (RS)-1-tert-Butoxyca

Isolation of Methyl (RS)-1-tert-Butoxycarbonyl-3-cyanomethyl-1,2-dihydro-2-oxo-5H-pyrrole-5- carboxylate, the Key-Intermediate in Base-Catalyzed Formation of Racemic Products by 1,3-Dipolar Cycloadditions to Methyl (S)-1-tert-Butoxycarbonyl-3- [(E)-cyanomethylidene]-2-pyrrolidinone-5-carboxylate.

✍ Marko Skof; Samo Pirc; Simon Recnik; Jurij Svete; Branko Stanovnik; Ljubo Golic; 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 185 KB 👁 2 views

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

Isolation of methyl (RS)-1-tert-butoxyca

Isolation of methyl (RS)-1-tert-butoxycarbonyl-3-cyanomethyl-1,2-dihydro-2-oxo-5H-pyrrole-5-carboxylate, the key-intermediate in base-catalyzed formation of racemic products by 1,3-dipolar cycloadditions to methyl (S)-1-tert-butoxycarbonyl-3-[(E)-cyanomethylidene]-2-pyrrolidinone-5-carboxylate

✍ Marko Škof; Samo Pirc; Simon Rečnik; Jurij Svete; Branko Stanovnik; Ljubo Golič; 📂 Article 📅 2002 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 81 KB

## Abstract Cycloadditions of various 1,3‐dipoles to methyl (__S__)‐1‐__tert__‐butoxycarbonyl‐3‐[(__E__)‐cyanomethylidene]‐2‐pyrrolidinone‐5‐carboxylate (**9**) were studied. Reactions of **9** with diazomethane (**10**) and 2,4,6‐trimethoxy‐benzonitrile oxide (**11**), carried out under neutral co