Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.14/11459
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- Title
- A novel reduction reaction for the conversion of aldehydes, ketones and primary, secondary and tertiary alcohols into their corresponding alkanes
- Related
- Tetrahedron letters, Vol. 47, Issue 32, p.5755-5758
- DOI
- 10.1016/j.tetlet.2006.06.007
- Publisher
- Elsevier Science
- Date
- 2006
- Author/Creator
- Nimmagadda, Rama D
- Author/Creator
- McRae, Christopher
- Description
- A novel one-pot reaction has been developed for the reduction of aldehydes, ketones and primary, secondary and tertiary alcohols into their corresponding alkyl function. This is also the first reported method which can efficiently reduce primary, secondary, or tertiary alcohols, without affecting carbon–carbon double bonds, into their corresponding alkyl function in high yields. The reduction utilises either diethylsilane or n-butylsilane as the reducing agent in the presence of the Lewis acid catalyst tris(pentafluorophenyl)borane.
- Description
- 4 page(s)
- Subject Keyword
- reduction
- Subject Keyword
- aldehydes
- Subject Keyword
- ketones
- Subject Keyword
- alcohols
- Subject Keyword
- DES : diethylsilane
- Subject Keyword
- n-BS : n-butylsilane
- Subject Keyword
- B(C₆F₅)₃ : tris(pentafluorophenyl)borane
- Resource Type
- journal article
- Organisation
- Macquarie University. Dept. of Chemistry and Biomolecular Sciences
- Identifier
- http://hdl.handle.net/1959.14/11459
- Identifier
- ISSN:1873-3581
- Identifier
- mq-rm-2006000545
- Language
- eng
- Reviewed
