1,2,4-Trioxane in organic synthesis. Unusual entry to diverse carbocyclic frameworks derived from β-ionone
摘要:
Synthesis of [4.4.0]- or [5.3.0]-bicyclic frameworks was achieved via sequential intramolecular Michael/aldol and tandem intramolecular adol/aldol strategies, starting from acyclic precursors derived from beta-ionone. (C) 2003 Elsevier Ltd. All rights reserved.
1,2,4-Trioxane in organic synthesis. Unusual entry to diverse carbocyclic frameworks derived from β-ionone
作者:Mirta Mischne
DOI:10.1016/s0040-4039(03)01404-7
日期:2003.7
Synthesis of [4.4.0]- or [5.3.0]-bicyclic frameworks was achieved via sequential intramolecular Michael/aldol and tandem intramolecular adol/aldol strategies, starting from acyclic precursors derived from beta-ionone. (C) 2003 Elsevier Ltd. All rights reserved.
Zur Kenntnis der 1,2-Epoxyde und verwandter Verbindungen
作者:P. Karrer、E. Rodmann
DOI:10.1002/hlca.19480310412
日期:——
Durch Oxydation von 2,3-Dioxy-2,3-dihydro-β-jonon mit Bleitetracetat wurde das 6-Dimethyl-undecen-(8)-trion-(2,7,10) dargestellt.