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Highly Enantioselective Intermolecular Hydroamination of Allylic Amines with Chiral Aldehydes as Tethering Catalysts
Chirally LinkedIn: Chiral aldehydes are effective tethering catalysts for enantioselective intermolecular hydroamination, which provides access to vicinal diamine motifs in good yields and excellent enantioselectivities (see scheme). This work highlights simple chiral α‐oxygenated aldehydes as effec...
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Published in: | Chemistry : a European journal 2013-02, Vol.19 (8), p.2597-2601 |
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container_end_page | 2601 |
container_issue | 8 |
container_start_page | 2597 |
container_title | Chemistry : a European journal |
container_volume | 19 |
creator | MacDonald, Melissa J. Hesp, Colin R. Schipper, Derek J. Pesant, Marc Beauchemin, André M. |
description | Chirally LinkedIn: Chiral aldehydes are effective tethering catalysts for enantioselective intermolecular hydroamination, which provides access to vicinal diamine motifs in good yields and excellent enantioselectivities (see scheme). This work highlights simple chiral α‐oxygenated aldehydes as effective organocatalysts capable of efficiently inducing asymmetry through transient intramolecularity. |
doi_str_mv | 10.1002/chem.201203462 |
format | article |
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subjects | Aldehydes Aldehydes - chemistry Alkenes - chemistry Amination Amines Amines - chemistry asymmetric catalysis Asymmetry Catalysis Catalysts Chemistry Diamines hydroamination hydroxylamines Stereoisomerism tethered reactions Tethering vicinal diamines |
title | Highly Enantioselective Intermolecular Hydroamination of Allylic Amines with Chiral Aldehydes as Tethering Catalysts |
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