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Synlett 2002(3): 0528-0530
DOI: 10.1055/s-2002-20487
DOI: 10.1055/s-2002-20487
LETTER
© Georg Thieme Verlag Stuttgart · New York
A Conceptually New and Straightforward Method for the One-pot Transformation of Alcohols into Amines
Further Information
Publication History
Received
18 December 2001
Publication Date:
05 February 2007 (online)


Abstract
A conceptually new amination method of alcohols has been developed using α-hydroxy esters as substrates and N-phenyl bis-trifluoromethanesulfonimide (PhNTf2) as a test reagent. Playing two roles at once, PhNTf2 activates the hydroxyl group as a highly reactive triflate intermediate and introduces the amino functionality through an in situ nucleophilic substitution by the anionic residue PhTfN-. Two complementary procedures (methods A and B herein) have been developed, the latter permitting reaction of substrates with unstable alcoxides.
Key words
amination - amino esters - nucleophilic substitution - triflate - one-pot