1. Synthetic studies aimed at the elucidation of the stereostructure of the aggregation pheromone, 2-methyl-6-(4′-methylenebicyclo[3.1.0]hexyl)hept-2-en-1-ol, produced by the male stink bug Erysarcoris lewisistar, open
Kenji Mori
Tetrahedron: Asymmetry
Volume 18, Issue 7, 30 April 2007, Pages 838-846
DOI:
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2007.03.019 Carlos Cativiela and María D. Díaz-de-Villegas
Tetrahedron: Asymmetry
Volume 18, Issue 5, 30 March 2007, Pages 569-623
DOI:
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2007.02.003 3. A facile asymmetric synthesis of (+)-eldanolide
Linglong Kong, Zeyang Zhuang, Qingshou Chen, Haibing Deng, Zhiyong Tang, Xueshun Jia, Yulin Li and Hongbin Zhai
Tetrahedron: Asymmetry
Volume 18, Issue 4, 12 March 2007, Pages 451-454
DOI:
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2007.01.035 Yui Masuda, Takuya Tashiro and Kenji Mori
Tetrahedron: Asymmetry
Volume 17, Issue 24, 27 December 2006, Pages 3380-3385
DOI:
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2006.12.025 Liang-Xian Liu, and Pei-Qiang Huang
Tetrahedron: Asymmetry
Volume 17, Issue 23, 11 December 2006, Pages 3265-3272
DOI:
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2006.12.009 6. A scalable and expedient method of preparing diastereomerically and enantiomerically enriched pseudonorephedrine from norephedrine
Jonathan A. Groeper, Shawn R. Hitchcock and Gregory M. Ferrence
Tetrahedron: Asymmetry
Volume 17, Issue 20, 6 November 2006, Pages 2884-2889
DOI:
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2006.11.007 7. Stereoselective synthesis of a C19–C26 fragment of amphidinolides G and H
Pilar Formentín, Juan Murga, Miguel Carda and J. Alberto Marco
Tetrahedron: Asymmetry
Volume 17, Issue 20, 6 November 2006, Pages 2938-2942
DOI:
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2006.10.024