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2001 amination, N-alkylation, N-arylation amination, N-alkylation, N-arylation O 0268 37 - 068 Highly Regio- and Enantioselective Palladium-Catalyzed Allylic Amination with Sodium Diformylamide. The resulting amines can easily be deprotected to primary allylic amines. Other advantages of the use of sodium diformylamide are high atom economy and its easy availability. (WANG, YI; DING, KUILING; J. Org. Chem. 66 (2001) 9, 3238-3241; Lab. Organomet. Chem., Shanghai Inst. Org. Chem., Acad. Sin., Shanghai 200032, Peop. Rep. China; EN) 1

ChemInform Abstract: Highly Regio- and Enantioselective Palladium-Catalyzed Allylic Amination with Sodium Diformylamide

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2001 amination, N-alkylation, N-arylation

amination, N-alkylation, N-arylationO 0268

37 - 068Highly Regio- and Enantioselective Palladium-Catalyzed AllylicAmination with Sodium Diformylamide. — The resulting amines caneasily be deprotected to primary allylic amines. Other advantages of the useof sodium diformylamide are high atom economy and its easy availability. —(WANG, YI; DING, KUILING; J. Org. Chem. 66 (2001) 9, 3238-3241; Lab.Organomet. Chem., Shanghai Inst. Org. Chem., Acad. Sin., Shanghai 200032,Peop. Rep. China; EN)

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