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|Title:||Enantioselective Synthesis of anti-β-Hydroxy-α-amino Esters via an Organocatalyzed Decarboxylative Aldol Reaction|
|Author's alias:||竹本, 佳司|
malonic acid half oxyester (MAHO)
|Publisher:||Georg Thieme Verlag|
|Abstract:||The first enantioselective decarboxylative aldol addition with α-amido-substituted malonic acid half oxyesters (MAHOs) is described. The combined use of a newly designed bifunctional sulfonamide catalyst with pentafluorobenzoic acid as an additive afforded the β-hydroxy-α-amino acid derivatives in moderate to high yields and with high enantioselectivities.|
|Rights:||This is the accepted manuscript of the article, which has been published in final form at http://doi.org/10.1055/s-0036-1588141|
The full-text file will be made open to the public on 2 March 2018 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.
This is not the published version. Please cite only the published version. この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。
|Appears in Collections:||Journal Articles|
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