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Efficient synthesis of dipeptide analogues of α-fluorinated β-aminophosphonates
Authors:
- Marcin Kaźmierczak,
- Henryk Koroniak
Abstract
Herein, we present an efficient synthesis of dipeptide analogues of α-fluorinated β-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. © 2020 Kaźmierczak and Koroniak;
- Record ID
- UAMb3ec0be4ab8a4af882959722bb037171
- Author
- Journal series
- Beilstein Journal of Organic Chemistry, ISSN 1860-5397
- Issue year
- 2020
- Vol
- 16
- Pages
- 756-762
- Keywords in English
- Dipeptide analogues; Fluorinated aminophosphonates; Fluorine; Nucleophilic fluorination; Phosphorus
- ASJC Classification
- DOI
- DOI:10.3762/bjoc.16.69 Opening in a new tab
- URL
- https://www.beilstein-journals.org/bjoc/articles/16/69/downloads Opening in a new tab
- Language
- (en) English
- Score (nominal)
- 70
- Score source
- journalList
- Score
- = 70.0, 11-02-2022, ArticleFromJournal
- Publication indicators
- = 1; = 2; : 2018 = 0.648; : 2019 (2 years) = 2.622 - 2019 (5 years) =2.406
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- Uniform Resource Identifier
- https://researchportal.amu.edu.pl/info/article/UAMb3ec0be4ab8a4af882959722bb037171/
- URN
urn:amu-prod:UAMb3ec0be4ab8a4af882959722bb037171
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