1. A Two-Step, Stereoselective Synthesis of Nine- and Ten-Membered Carbocycles from Phthalates
- Author
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M. Rita Paleo, Gustavo Prado, Alberte X. Veiga, F. Javier Sardina, Fernando Fernández-Nieto, Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares, and Universidade de Santiago de Compostela. Departamento de Química Orgánica
- Subjects
Bicyclic molecule ,Chemistry ,Organic Chemistry ,Two step ,Organic chemistry ,Stereoselectivity ,Physical and Theoretical Chemistry ,Biochemistry ,Bond cleavage - Abstract
A two-step, stereoselective procedure for the synthesis of nine- and ten-membered carbocycles from readily available phthalates is described. A variety of dialkyl phthalates have been transformed into [6,n]-fused bicyclo systems (n = 5, 6, 7) by a dearomatization/cyclization process and then converted into cyclonona- and cyclodecadienes through a bond cleavage reaction, whereby both processes are promoted by alkaline metals in THF This work was supported by the Spanish MINECO (CTQ2011-22436), and the Xunta de Galicia (GRC2014/029) SI
- Published
- 2015