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All posts Subject: Imines from alcohols in one pot. Please login to post

Rhodium
(Chief Bee)
01-26-04 06:46
No 484617
User Picture Imines from alcohols in one pot.
(Rated as: good read)

In Situ Oxidation-Imine Formation-Reduction Routes from Alcohols to Amines
Leonie Blackburn and Richard J. K. Taylor
Org. Lett. 3(11) 1637-1639 (2001) (https://www.rhodium.ws/pdf/alcohol2amine.pscbh.pdf)
DOI:10.1021/ol015819b

Abstract
Manganese dioxide is employed as an in situ oxidant for the one-pot conversion of alcohols into imines. In combination with polymersupported cyanoborohydride (PSCBH), a one-pot oxidation-imine formation-reduction sequence is reported. This procedure enables alcohols to be converted directly into both secondary and tertiary amines.

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	All posts		Subject: Imines from alcohols in one pot.		Please login to post


		Rhodium (Chief Bee) 01-26-04 06:46 No 484617				Imines from alcohols in one pot. (Rated as: good read)
						In Situ Oxidation-Imine Formation-Reduction Routes from Alcohols to Amines Leonie Blackburn and Richard J. K. Taylor Org. Lett. 3(11) 1637-1639 (2001) (https://www.rhodium.ws/pdf/alcohol2amine.pscbh.pdf) DOI:10.1021/ol015819b Abstract Manganese dioxide is employed as an in situ oxidant for the one-pot conversion of alcohols into imines. In combination with polymersupported cyanoborohydride (PSCBH), a one-pot oxidation-imine formation-reduction sequence is reported. This procedure enables alcohols to be converted directly into both secondary and tertiary amines. ^{The Hive - Clandestine Chemists Without Borders}

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