A Direct and Stereoretentive Synthesis of Amides from Cyclic Alcohols
β Scribed by Deboprosad Mondal; Luca Bellucci; Salvatore D. Lepore
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 416 KB
- Volume
- 2011
- Category
- Article
- ISSN
- 1434-193X
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## Abstract Amides are synthesized directly from alcohols and amines in high yields using an __in situ__ generated catalyst from easily available ruthenium complexes such as the (__p__βcymene)ruthenium dichloride dimer, [Ru(__p__βcymeme)Cl~2~]~2~, or the (benzene)ruthenium dichloride dimer, [Ru(ben
Synthesis of Cyclic Depsipeptides and Peptides via Direct Amide Cyclization. -An excellent preparative route to ten-membered peptides is presented consisting of the combination of the so-called azirine/oxazolone method and the acid catalyzed amide cyclization. -(VILLALGORDO, J.
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