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Volumn 61, Issue 23, 2005, Pages 5465-5473

Conformationally restricted analogues of both (S)-β-homoserine and (S)-aspartic acid from chiral 3-acylamino pyrrolidin-2-ones

Author keywords

Amino acids; Analogues; Baylis Hillman; Conformational constrictions; Peptidomimetics

Indexed keywords

3 ACYLAMINOPYRROLIDIN 2 ONE; ASPARTIC ACID; HOMOSERINE; UNCLASSIFIED DRUG;

EID: 19044390133     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.03.129     Document Type: Article
Times cited : (35)

References (69)
  • 39
    • 19044391701 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra the signals corresponding to each isomer could be identified. In contrast, treatment of the diastereomeric mixture of 3-tosylamino derivatives with DBU led exclusively to the corresponding α,β- unsaturated pyrrolidin-2-one in a quantitative yield, via elimination of tosylamide.
  • 40
    • 0004150157 scopus 로고    scopus 로고
    • University of Gottingen, Germany
    • Sheldrick, G. M. SHELXS97, University of Gottingen, Germany, 1997.
    • (1997) SHELXS97
    • Sheldrick, G.M.1
  • 41
    • 0004150157 scopus 로고    scopus 로고
    • University of Gottingen, Germany
    • Sheldrick, G. M. SHELXL97, University of Gottingen, Germany, 1997.
    • (1997) SHELXL97
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.