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Volumn , Issue 3, 2011, Pages 607-613

1,3-dipolar cycloaddition of azomethine ylides to aldehydes: Synthesis of anti α-amino-β-hydroxy esters

Author keywords

Aldehydes; Amino alcohols; Azomethine ylides; Cycloaddition

Indexed keywords


EID: 78651330597     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001274     Document Type: Article
Times cited : (20)

References (31)
  • 2
    • 0004101860 scopus 로고
    • A. Padwa (Ed.), Wiley, New York, vol. 2.
    • A. Padwa (Ed.), 1,3-Dipolar Cycloaddition Chemistry, Wiley, New York, 1984, vol. 2.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry
  • 25
    • 78651341068 scopus 로고    scopus 로고
    • the coupling constant of the trans oxazolidinone derived from amino alcohol 12b was found to be 3.8 Hz
    • the coupling constant of the trans oxazolidinone derived from amino alcohol 12b was found to be 3.8 Hz.
  • 26
    • 78651305641 scopus 로고    scopus 로고
    • Byproduct 11 is proposed to arise from protonation of the AMY followed by hydrolysis
    • Byproduct 11 is proposed to arise from protonation of the AMY followed by hydrolysis.
  • 27
    • 78651290769 scopus 로고    scopus 로고
    • note
    • The relative stereochemistries of 10a-c were assigned as follows: 10b and 10c both yield 12b upon hydrolysis and are thus C-2 epimers; the C-2 relative stereochemistries for these compounds were arbitrarily assigned. Hydrolysis of 10a yields 12a and must then be C-4/C-5 syn, whereas the C-2 relative stereochemistry was arbitrarily assigned.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.