A one-pot tandem oxidation-reduction protocol for the synthesis of cyclic ethers from their diols

Tetrahedron Letters

Volumn 49, Issue 47, 2008, Pages 6701-6703

  Panda, Biswajit ^a   Sarkar, Tarun K ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; ETHER DERIVATIVE; MANGANESE DIOXIDE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHROMATOGRAPHY; CYCLIZATION; ETHERIFICATION; ONE POT SYNTHESIS; OXIDATION REDUCTION REACTION;

EID: 53149090501     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.09.046     Document Type: Article

References (14)

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10. 13 C NMR spectroscopy as well as mass spectral data.
11. All reactions were carried out on a 1 mmol scale.
12. 3, 50 MHz) δ 162.4, 151.7, 139.9, 130.3, 122.2, 73.3, 71.5.
13. 2 prepared in this way was further dried at 120 °C overnight everytime before use
14. Publications on the synthesis of acyclic ethers via reductive etherification of carbonyl compounds with alkoxysilanes and triethylsilane promoted by Lewis acids are numerous, see:. Iwanami K., Seo H., Tobita Y., and Oriyama T. Synthesis (2005) 183 and references cited therein