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Volumn 23, Issue 11, 1984, Pages 898-899

Highly Enantioselective Homoaldol Additions with Chiral N‐Allylureas—Application to the Synthesis of Optically Pure γ‐Lactones

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Indexed keywords


EID: 84985560842     PISSN: 05700833     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.198408981     Document Type: Article
Times cited : (112)

References (22)
  • 1
    • 84918427926 scopus 로고
    • syn-Diastereoselektive Homoaldol-Reaktionen: γ-Hydroxyalkylierung von (Z)-2-Butenylcarbamaten und Synthese von β,γ-cis-di- und -trisubstituierten γ-Lactonen
    • (1984) Angewandte Chemie , vol.96 , pp. 241
    • Hoppe, D.1    Lichtenberg, F.2
  • 14
    • 0000034230 scopus 로고
    • This reaction has already been performed with (±)‐ephedrine, but on the basis of mechanistic considerations, the product was incorrectly assigned the trans‐configuration
    • (1950) J. Org. Chem. , vol.15 , pp. 1131
    • Close, W.J.1
  • 18
    • 84985558499 scopus 로고    scopus 로고
    • 2O exhibits high γ‐regioselectively but no stereoselectivity.
  • 22
    • 84985529522 scopus 로고    scopus 로고
    • The change in the notation for the absolute configuration in the series 8a‐d and 10a, b, d (cf. Table 2) is determined by the alteration in the substituent priorities.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.