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Pure Appl. Chem., 2008, Vol. 80, No. 4, pp. 681-685

N,O-Heterocycles as synthetic intermediates

Roderick W. Bates, Jutatip Boonsombat, Yongna Lu, Joseph A. Nemeth, Kanicha Sa-Ei, Ping Song, Melody Peiling Cai, Philippa B. Cranwell and SusAnn Winbush

Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, 637371, Singapore

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  • Gimeno Ana, Cuenca Ana B., Medio-Simón Mercedes, Asensio Gregorio: Gold(I)-Catalyzed Reactions of 1-(ortho -Alkynylaryl)ureas: Highly Selective Heterocyclization and Synthesis of Mixed N ,O -Acetals. Adv. Synth. Catal. 2014, 356, 229. <>
  • Malkov Andrei V., Lee Darren S., Barłóg Maciej, Elsegood Mark R. J., Kočovský Pavel: Palladium-Catalyzed Stereoselective Intramolecular Oxidative Amidation of Alkenes in the Synthesis of 1,3- and 1,4-Amino Alcohols and 1,3-Diamines. Chem. Eur. J. 2014, n/a. <>
  • Bates Roderick W., Aslam Nur Filza bte Mohamed, Tang Chi H., Simon Oliver: A synthesis of 5-hydroxysedamine using hydroformylation. Tetrahedron 2014, 70, 2134. <>
  • Malkov Andrei V., Barłóg Maciej, Miller-Potucká Lucie, Kabeshov Mikhail A., Farrugia Louis J., Kočovský Pavel: Stereoselective Palladium-Catalyzed Functionalization of Homoallylic Alcohols: A Convenient Synthesis of Di- and Trisubstituted Isoxazolidines and β-Amino-δ-Hydroxy Esters. Chem. Eur. J. 2012, 18, 6873. <>
  • Doyle Linda, Heaney Frances: An investigation of structure-reactivity relationships of δ-alkenyl oximes; competitive thermal reactions leading to cyclic nitrones and/or N-unsubstituted bicyclic isoxazolidines. Tetrahedron 2010, 66, 7041. <>
  • Bates Roderick W., Lu Yongna, Cai Melody Peiling: Ring opening of cyclic N,O-acetals with allyltrimethylsilane under Lewis acidic conditions. Tetrahedron 2009, 65, 7852. <>
  • Bates Roderick W., Boonsombat Jutatip, Lu Yongna, Nemeth Joseph A., Sa-Ei Kanicha, Song Ping, Cai Melody Peiling, Cranwell Philippa B., Winbush SusAnn: ChemInform Abstract: N,O-Heterocycles as Synthetic Intermediates. ChemInform 2008, 39. <>