4.5 Article

Efficient synthesis of dipeptide analogues of α-fluorinated β-aminophosphonates

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 16, 期 -, 页码 756-762

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.16.69

关键词

dipeptide analogues; fluorinated aminophosphonates; fluorine; nucleophilic fluorination; phosphorus

资金

  1. National Science Centre [2018/02/X/ST5/02867]

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Herein, we present an efficient synthesis of dipeptide analogues of alpha-fluorinated beta-aminophosphonates. Each step of the synthesis was optimized to provide excellent yields. Moreover, the absolute configuration of the obtained compounds was determined by X-ray analysis, which proved the stereochemistry that was proposed based on NMR studies.

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