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Volumn 70, Issue , 2006, Pages 223-233

A de novo asymmetric approach to achiral deoxy-melodorinol analogues

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EID: 33947625156     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-06-s(w)12     Document Type: Article
Times cited : (5)

References (24)
  • 1
    • 33947642174 scopus 로고    scopus 로고
    • note
    • This paper is dedicated to Professor Steven Weinreb on the occasion of his 65th birthday.
  • 10
    • 33746314617 scopus 로고    scopus 로고
    • For other examples of anti-eliminations see:
    • For other examples of anti-eliminations see:. Olpp T., and Brückner R. Angew. Chem., Int. Ed. 45 (2006) 4023
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 4023
    • Olpp, T.1    Brückner, R.2
  • 19
    • 28744436768 scopus 로고    scopus 로고
    • Previously, we have shown that Z,E-dienoate spontaneously lactonize after dihydroxylation, see:
    • Previously, we have shown that Z,E-dienoate spontaneously lactonize after dihydroxylation, see:. Ahmed M.M., and O'Doherty G.A. J. Org. Chem. 67 (2005) 10576
    • (2005) J. Org. Chem. , vol.67 , pp. 10576
    • Ahmed, M.M.1    O'Doherty, G.A.2
  • 20
    • 85086795317 scopus 로고    scopus 로고
    • note
    • 2O).
  • 21
    • 33947678305 scopus 로고    scopus 로고
    • note
    • Compounds (1a, 2a and 3a) are known compounds and procedures for their preparation can be found in refs. 12-14.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.