1. Tetrahedron: Asymmetry
Volume 20, Issue 16, 26 August 2009, Pages 1940-1947
Giuseppe Cremonesi, Piero Dalla Croce, Alessandra Forni, Maddalena Gallanti, Raffaella Gandolfi and Concetta La Rosa
Enzymatic resolution of (±)-5-phenyl-4,5-dihydroisoxazole-3-carboxylic acid ethyl ester and its transformations into polyfunctionalised amino acids and dipeptides
Код: Выделить всё
dx.doi.org/10.1016/j.tetasy.2009.07.025Volume 12, Issue 1, 2 January 2004, Pages 191-197
Zoia Mincheva, Martine Courtois, Joel Creche, Marc Rideau and Marie-Claude Viaud-Massuard
One-pot synthesis of functionalized 4,5-dihydroisoxazole derivatives via nitrile oxides and biological evaluation with plant cells
Код: Выделить всё
dx.doi.org/10.1016/j.bmc.2003.10.0083. Tetrahedron Letters
Volume 46, Issue 38, 19 September 2005, Pages 6563-6566
Agnieszka Cwik, Zoltan Hell, Aliz Fuchs and Dora Halmai
Solid base-catalyzed synthesis of 5-substituted 4,5-dihydroisoxazoles
Код: Выделить всё
dx.doi.org/10.1016/j.tetlet.2005.07.071Volume 50, Issue 40, 7 October 2009, Pages 5647-5648
Michael D. Mosher, Amber L. Norman and Khriesto A. Shurrush
5-Bromomethyl-4,5-dihydroisoxazoles
Код: Выделить всё
dx.doi.org/10.1016/j.tetlet.2009.07.106Volume 19, Issue 24, 12 December 2008, Pages 2850-2855
Giuseppe Cremonesi, Piero Dalla Croce, Francesco Fontana, Claudio Fiorelli and Concetta La Rosa
Stereoselective synthesis of b,e-dihydroxy-a-amino acids by ring opening of 4,5-dihydroisoxazolyl derivatives
Код: Выделить всё
dx.doi.org/10.1016/j.tetasy.2008.11.034Volume 40, Issue 47, 19 November 1999, Pages 8295-8298
William M. Horspool, George Hynd and Ulrich Ixkes
SET induced cyclizations of b,g-unsaturated oximes. A novel photochemical route to dihydroisoxazole derivatives
Код: Выделить всё
dx.doi.org/10.1016/S0040-4039(99)01759-1Volume 58, Issue 47, 18 November 2002, Pages 9613-9620
Akio Kamimura, , a, Yukio Kanekoa, Ayaki Ohtaa, Kenji Matsuuraa, Yasuo Fujimotoa, Akikazu Kakehib and Shuji Kanemasa
Enantioselective preparation of 3,4,5-trisubstituted 4,5-dihydroisoxazoles and their stereoselective elaboration of 5-side chain
Код: Выделить всё
dx.doi.org/10.1016/S0040-4020(02)01255-3
