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Volumn 24, Issue 22, 1983, Pages 2231-2234

Stereochemistry of Vinyl Cuprate Additions to Carbohydrate-Derived Enones and α,β-Unsaturated Esters

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Indexed keywords


EID: 0001592452     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)81891-2     Document Type: Article
Times cited : (94)

References (27)
  • 13
    • 84919015449 scopus 로고    scopus 로고
    • 2. These reactions were more selective for the (Z)-isomers when performed in methanol.
  • 14
    • 84919015448 scopus 로고    scopus 로고
    • (a) The spectroscopic properties (NMR, IR, mass spectrum) of all new compounds are fully consistent with the assigned structures; (b) A satisfactory combustion analysis (±0.3% for C,H) was obtained for this compound; (c) The elemental composition of this substrate was confirmed by high resolution mass spectroscopy.
  • 18
    • 84919015447 scopus 로고    scopus 로고
    • The epimer of 6 was not detected in the sentence 4 → 5 → 6. It may have been separated inadvertently during the purification of 5.
  • 21
    • 84919015446 scopus 로고    scopus 로고
    • 2, 20°C).
  • 22
    • 84919015445 scopus 로고    scopus 로고
    • 3 also provided much useful information.
  • 23
    • 84919015444 scopus 로고    scopus 로고
    • 2O, .
  • 24
    • 49949128203 scopus 로고
    • Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones
    • (1968) Tetrahedron Letters , pp. 2199
    • Chérest1    Felkin2    Prudent3
  • 25
    • 0001432464 scopus 로고
    • Similar arguments based on the anti-periplanar effect have recently been invoked by Koqikowski and Franck to rationalize the stereochemistry of nitrile oxide and Diels-Alder reactions of alkoxy-functionalized allylic systems:
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5788
    • Kozikowski1    Ghosh2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.