An economic and practical synthesis of the 2-tetrahydrofuranyl ether protective group

Tetrahedron Letters

Volumn 47, Issue 29, 2006, Pages 5111-5113

  Falck, J R ^a   Li, De Run ^a   Bejot, Romain ^b   Mioskowski, Charles ^b  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

Manganese; Protecting group; Radical reaction; Tetrahydrofuran

Indexed keywords

ALCOHOL; CARBOHYDRATE; CARBON TETRACHLORIDE; ETHER DERIVATIVE; MANGANESE; PHENOL; TETRAHYDROFURAN;

ARTICLE; CHEMICAL STRUCTURE; COST BENEFIT ANALYSIS; ETHERIFICATION; POWDER; REACTION ANALYSIS; SYNTHESIS;

EID: 33744976358     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.05.081     Document Type: Article

References (16)

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2. THF ethers can be selectively cleaved in the presence of THP ethers, for example, see Refs. 1,3.
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14. Mn(0) powder was purchased from Aldrich Chem. (99%, -325 mesh). While it could be weighed and handled without special precautions, it was stored under an inert atmosphere to help retain its full reactivity.
15. 3 (M+1) m/e 373.2743, found 373.2740.
16. Takai K., Ueda T., Ikeda N., Ishiyama T., and Matsushita H. Bull. Chem. Soc. Jpn. 76 (2003) 347-353