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Volumn , Issue 10, 2013, Pages 1884-1888

Stereoselective Synthesis of (E)-α,β-dehydroamino acid esters

Author keywords

Aldehydes; Amino acids; Metal additive effects; Olefination

Indexed keywords


EID: 84875452154     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201300112     Document Type: Article
Times cited : (14)

References (36)
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    • 16644369699 scopus 로고    scopus 로고
    • The E/Z ratio was determined by comparison of the NMR spectroscopic data (olefinic proton, -NH, ester methyl group). This data is summarized in the Supporting Information. In most of the cases, the olefinic protons of (E)- 1 were observed at lower magnetic field than those of (Z)- 2. The tendency is consistent with the data reported by Mazurkiewicz et al., see.
    • The E/Z ratio was determined by comparison of the NMR spectroscopic data (olefinic proton, -NH, ester methyl group). This data is summarized in the Supporting Information. In most of the cases, the olefinic protons of (E)- 1 were observed at lower magnetic field than those of (Z)- 2. The tendency is consistent with the data reported by Mazurkiewicz et al., see:, R. Mazurkiewicz, A. Kuźnik, M. Grymel, N. Kuźnik, Magn. Reson. Chem. 2005, 43, 36-40.
    • (2005) Magn. Reson. Chem. , vol.43 , pp. 36-40
    • Mazurkiewicz, R.1    Kuźnik, A.2    Grymel, M.3    Kuźnik, N.4
  • 36
    • 84875452444 scopus 로고    scopus 로고
    • This method has been successfully extended to the synthesis of phosphonoglycinate derivatives possessing an amino acid residue in the amino group. Full details and synthetic applications will be reported in due course
    • This method has been successfully extended to the synthesis of phosphonoglycinate derivatives possessing an amino acid residue in the amino group. Full details and synthetic applications will be reported in due course.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.