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Volumn 4, Issue 6, 2002, Pages 893-896

Turn formation initiated by a bissulfoximine motif: Synthesis and structural investigation

Author keywords

[No Author keywords available]

Indexed keywords

IMINE;

EID: 0037149654     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol017188r     Document Type: Article
Times cited : (43)

References (36)
  • 8
    • 0000219483 scopus 로고
    • Symposia-in-Print, no. 50
    • (a) For reviews on peptide secondary structure mimetics, see: Tetrahedron (Symposia-in-Print, no. 50; Kahn, M., Ed.) 1993, 49, 3433.
    • (1993) Tetrahedron , vol.49 , pp. 3433
    • Kahn, M.1
  • 23
  • 25
    • 0033985468 scopus 로고    scopus 로고
    • Sulfoximines can easily be prepared on a multigramm scale. For a recent review, see: Reggelin, M.; Zur, C. Synthesis 2000, 1.
    • (2000) Synthesis , pp. 1
    • Reggelin, M.1    Zur, C.2
  • 28
    • 0000960154 scopus 로고
    • Sulfoximine 6 is commercially available in both enantiomeric forms. Alternatively, it can easily be synthesized following protocols described in: (a) Johnson, C. R.; Schroeck, C. W. J. Am. Chem. Soc. 1973, 95, 7418.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 7418
    • Johnson, C.R.1    Schroeck, C.W.2
  • 36
    • 0030599269 scopus 로고    scopus 로고
    • The E/Z ratio was approximately 1.6:1, which is similar to the ones reported for macrocyclizations by RCM. Fürstner, A.; Kindler, N. Tetrahedron Lett. 1996, 37, 7005.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7005
    • Fürstner, A.1    Kindler, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.