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Synthesis of cyclodeca-1,5-diyne derivatives having o-nitrophenylseleno group
M Michida1, K Sakagami, T Shimono
1Department of Chemistry, College of Science and Engineering, Aoyama Gakuin University, Tokyo, Japan.
Nucleic Acids Symposium Series
|January 1, 1997
Abstract:
7-Benzoyloxy-3-(2-nitrophenylseleno)-1,5-cyclodecadiyne (13) was prepared from 5-hexyn-1-ol and propargyl bromide via 10-iodo-7-(t-butyldiphenylsiloxy)-5,9-decadiynal (10). The facile cyclization of the acyclic precursor 10 would be rationalized in terms of "bulky group (TBDPSO) assisted conformational control". Oxidation of 13 by NaIO4, followed by thermal treatment gave tetrahydronaphthalene derivative 15, indicating the generation of biradical.