Pure Appl. Chem., 2008, Vol. 80, No. 4, pp. 681-685
http://dx.doi.org/10.1351/pac200880040681
N,O-Heterocycles as synthetic intermediates
CrossRef Cited-by Linking
- 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. <http://dx.doi.org/10.1002/adsc.201300730>
- 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. <http://dx.doi.org/10.1002/chem.201400123>
- Bates Roderick W., Aslam Nur Filza bte Mohamed, Tang Chi H., Simon Oliver: A synthesis of 5-hydroxysedamine using hydroformylation. Tetrahedron 2014, 70, 2134. <http://dx.doi.org/10.1016/j.tet.2014.02.001>
- 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. <http://dx.doi.org/10.1002/chem.201102716>
- 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. <http://dx.doi.org/10.1016/j.tet.2010.06.005>
- 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. <http://dx.doi.org/10.1016/j.tet.2009.07.011>
- 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. <http://dx.doi.org/10.1002/chin.200838252>