4.7 Article

Synthesis of N-Fmoc-(2S,3S,4R)-3,4-dimethylglutamine:: An application of lanthanide-catalyzed transamidation

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 70, Issue 16, Pages 6218-6221

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo050518r

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Funding

  1. NIAID NIH HHS [R01 AI050888-04, AI-50888, R01 AI050888] Funding Source: Medline

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N-Fmoc-(2S,3S,4R)-3,4-dimethylglutamine (6) was synthesized from tert-butyl N-Boc-(2S,3S,4R)dimethylpyroglutamate (13). This synthesis involved selective deprotection of a Boc group from a lactam nitrogen in the presence of a tert-butyl ester, Fmoc protection of the lactam, and a lanthanidecatalyzed transamidation reaction of the Fmoc-protected lactam, using ammonia and dimethylaluminum chloride. The scope of Lewis acid-catalyzed transamidation of acylated lactams was explored through the variation of lanthanide, lactam, acyl group, amine, and aluminum reagent. The reactivity of various metal triflates was found to vary in the following qualitative order: Yb Sc > Er similar to Eu similar to Sm > Ce similar to Agl > Cu-II similar to Zn. Intriguingly, catalysis was only observed when ammonia was the nitrogen nucleophile; addition of other amidoaluminum complexes to acyl lactams was found to be insensitive to the addition of lanthanides.

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