A Novel Dimer of ?-Tocopherol

Clicks: 168
ID: 10984
2008
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Abstract
Decomposition of the complex 4, formed between the ?-tocopherol ortho-quinone methide (2) and NMMO, by fast heating from −78∘C to 70∘C in inert solvents produces a novel ?-tocopherol dimer with 6?,12?-dibenzo[b,f][1,5]dioxocine structure (5) which—in contrast to the well-known spiro-dimer of ?-tocopherol (3)—is symmetrical. This is the first example of a direct reaction of the highly transient zwitterionic, aromatic precursor 2a in the formation of the ortho-quino
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anjan2008aorganic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Patel, Anjan;Mazzini, Francesco;Netscher, Thomas;Rosenau, Thomas;Patel, Anjan;Mazzini, Francesco;Netscher, Thomas;Rosenau, Thomas;
Journal organic chemistry international
Year 2008
DOI
10.1155/2008/742590
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