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Volumn 17, Issue , 1997, Pages 73-107

Reductive opening of saturated oxa-, aza- and thia-cycles by means of an arene-promoted lithiation: Synthetic applications

Author keywords

Functionalization; Heterocycles; Lithiation; Reductive opening

Indexed keywords


EID: 0001820427     PISSN: 09156151     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (132)

References (101)
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    • Gray, M.1    Tinkl, M.2    Snieckus, V.3
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    • note
    • nLi followed by addition of chloromethyl methyl ether at -78°C.
  • 58
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    • note
    • 20)
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    • (1989)
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    • note
    • Aziridines 5f and 5g were prepared starting from (-)-ephedrine by tandem chlorination-intramolecular cyclization and using a Mitsunobutype reaction, respectively.
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    • For reviews, see: (a) N. H. Werstiuk: Tetrahedron 39 205-268 (1983).
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    • (Eds.) B. M. Trost, I. Fleming and C. H. Heathcock Pergamon Press, Oxford
    • (c) I. Kuwajima and E. Nakamura: Comprehensive Organic Synthesis, (Eds.) B. M. Trost, I. Fleming and C. H. Heathcock (Pergamon Press, Oxford, 1991) Vol. II, pp. 441-473.
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    • Kuwajima, I.1    Nakamura, E.2
  • 100


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.