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Volumn 47, Issue 23, 2011, Pages 6569-6571

A one-pot, reductive amination/6-endo-trig cyclisation for the stereoselective synthesis of 6-substituted-4-oxopipecolic acids

Author keywords

[No Author keywords available]

Indexed keywords

4 OXO PIPECOLIC ACID; CYANOBOROHYDRIDE SODIUM; PIPECOLIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79957974149     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c1cc11916h     Document Type: Article
Times cited : (21)

References (38)
  • 37
    • 0027934159 scopus 로고
    • A direct 6-endo-trig cyclisation of trityl protected enones 7 and 10 as well as the corresponding free amino and Boc-protected compounds under acid, Lewis acid or base-mediated conditions was initially attempted. However, these reactions either returned starting material or generated a complex mixture of products See supporting information for NOE experiments for compounds 23, 24, 25 and 26 Due to a reversal of priority at C-6, the absolute configuration of 26 is (2S,4S,6S)
    • D. E. Rudisill J. P. Whitten Synthesis 1994 851
    • (1994) Synthesis , pp. 851
    • Rudisill, D.E.1    Whitten, J.P.2
  • 38
    • 33748542524 scopus 로고
    • 2 = 0.0639 for all data, reflections collected/unique 8583/2148. Supplementary crystallographic data have been deposited at the Cambridge Crystallographic Data Centre, CCDC
    • F. Johnson Chem. Rev. 1968 68 375
    • (1968) Chem. Rev. , vol.68 , pp. 375
    • Johnson, F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.