Metal-free catalysis: Highly functionalized molecules with two contiguous stereocenters are easily accessed in high yield with high enantio- and diastereoselectivity by using a commercially available organocatalyst ((DHQD)2PYR, see scheme). The easily removed Boc protecting group in the product is an added value to this method as an important tool in asymmetric synthesis.

Direct organocatalytic and highly enantio- and diastereoselective Mannich reactions of alpha-substituted alpha-cyanoacetates / Poulsen, Tb; Alemparte, C; Saaby, S; Bella, Marco; Jorgensen, Ka. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION. - ISSN 1433-7851. - 44:(2005), pp. 2896-2899. [10.1002/anie.200500144]

Direct organocatalytic and highly enantio- and diastereoselective Mannich reactions of alpha-substituted alpha-cyanoacetates

BELLA, Marco;
2005

Abstract

Metal-free catalysis: Highly functionalized molecules with two contiguous stereocenters are easily accessed in high yield with high enantio- and diastereoselectivity by using a commercially available organocatalyst ((DHQD)2PYR, see scheme). The easily removed Boc protecting group in the product is an added value to this method as an important tool in asymmetric synthesis.
2005
Asymmetric Organocatalysis; Mannich Reaction
01 Pubblicazione su rivista::01a Articolo in rivista
Direct organocatalytic and highly enantio- and diastereoselective Mannich reactions of alpha-substituted alpha-cyanoacetates / Poulsen, Tb; Alemparte, C; Saaby, S; Bella, Marco; Jorgensen, Ka. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION. - ISSN 1433-7851. - 44:(2005), pp. 2896-2899. [10.1002/anie.200500144]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/131564
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