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Volumn 40, Issue 3, 1999, Pages 467-470

A novel, one-pot preparation of N-methyl-α-amino acid dipeptides from oxazolidinones and amino acids

Author keywords

[No Author keywords available]

Indexed keywords

DIPEPTIDE; N HYDROXYMETHYLDIPEPTIDE; N METHYL ALPHA AMINO ACID DIPEPTIDE; OXAZOLIDINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033556071     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02426-5     Document Type: Article
Times cited : (16)

References (22)
  • 18
    • 0013469852 scopus 로고    scopus 로고
    • note
    • (b) The oxazolidinones were prepared by adding 3 equiv of trioxane and 0.6 equiv of p-toluenesulfonic acid to the N-Cbz-α-amino acid in toluene. The slurry was refluxed for 4 h giving a homogeneous solution which was worked-up following Ben-Ishai's procedure.
  • 20
    • 0013470681 scopus 로고    scopus 로고
    • note
    • 13C NMR, MS, IR, rotation, and combustion analysis.
  • 22
    • 0013510758 scopus 로고    scopus 로고
    • All of our attempts to determine the chiral integrity of the dipeptides by HPLC have been unsuccessful to date
    • All of our attempts to determine the chiral integrity of the dipeptides by HPLC have been unsuccessful to date.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.