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Volumn 71, Issue 13, 2006, Pages 4969-4979

Stereoselective synthesis of (Z)-alkene-containing proline dipeptide mimetics

Author keywords

[No Author keywords available]

Indexed keywords

(Z)-ALKENE DIPEPTIDE MIMETICS; AMIDE BOND; CYCLIC STRUCTURE; SYNTHETIC METHODOLOGY;

EID: 33745460391     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0606002     Document Type: Article
Times cited : (27)

References (77)
  • 42
    • 33745437197 scopus 로고    scopus 로고
    • note
    • Amino alcohol 10, which was gradually decomposed at room temperature, was converted to more stable derivative 11 by O-TBS protection.
  • 51
    • 33745460075 scopus 로고    scopus 로고
    • note
    • Phosphate 4b, which was easily obtainable by synthetic manipulations similar to those of 4a, was also used as a substrate in Table 1 to explore the suitable synthetic route to the desired isostere.
  • 55
    • 0027271839 scopus 로고
    • (b) Wipf, P. Synthesis 1993, 6, 537-557.
    • (1993) Synthesis , vol.6 , pp. 537-557
    • Wipf, P.1
  • 57
    • 0000453552 scopus 로고
    • 2), respectively, as a matter of convenience. For the discussion about the structure of the copper reagents, see: (a) Bertz, S. H. J. Am. Chem. Soc. 1990, 112, 4031-4032.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 4031-4032
    • Bertz, S.H.1
  • 77
    • 33745438496 scopus 로고    scopus 로고
    • note
    • Exposure of 8a to the N-Boc protection reaction conditions induced no epimerization at the 4-position on the isostere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.