Simple and Efficient One-Pot Synthesis of Nitriles from Amides and Oximes Using in Situ–Generated Burgess-Type Reagent
Author:
Affiliation:
1. a Department of Applied Chemistry , Cochin University of Science and Technology , Cochin , Kerala , India
2. b Department of Chemistry , Government Victoria College , Palakkad , Kerala , India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2010.515333
Reference15 articles.
1. The reactions of an N-sulfonylamine inner salt
2. Unexpected Formation of an Azetidine−Carborane Derivative by Dehydration of N-(1,12-Dicarba-closo-dodecaboran-1-yl)formamide. The First X-ray Structure of a 2,3-Bis(imino)azetidine
3. A Novel Regio- and Stereoselective Synthesis of Sulfamidates from 1,2-Diols Using Burgess and Related Reagents: A Facile Entry into β-Amino Alcohols We thank Professor K. Barry Sharpless for the gracious donation of several of the starting diol substrates. We also thank Drs. D. H. Huang, G. Suizdak, and R. Chadja for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, predoctoral fellowships from the National Science Foundation and Pfizer (S.A.S.), a postdoctoral fellowship from The Skaggs Institute for Chemical Biology (X.H.), and grants from American Biosciences, Amgen, Array Biopharma, Boehringer-Ingelheim, Glaxo, Hoffman-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
4. One-pot easy conversion of Baylis–Hillman adducts into carbamates of unsaturated β-amino acids
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