메뉴 건너뛰기




Volumn 27, Issue 31, 1986, Pages 3595-3598

Diastereoselective synthesis of 2,3,4-trisubstituted γ-lactols and γ-lactones via regio- and stereocontrolled opening of a 1,2-epoxy-4-hydroxyalkyl carbamate with hetero-nucleophiles

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0008307812     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)84858-3     Document Type: Article
Times cited : (16)

References (18)
  • 1
    • 84918462812 scopus 로고    scopus 로고
    • D. Hoppe, J. Lüßmann, P. G. Jones, D. Schmidt, G. M. Sheldrick, Tetrahedron Lett. 26, preceding communication.
  • 2
    • 0000163012 scopus 로고
    • Die Homoaldol-Reaktion oder wie man Probleme der Regio- und Stereoselektivität in den Griff bekommt
    • Review
    • (1984) Angewandte Chemie , vol.96 , pp. 930
    • Hoppe1
  • 9
    • 84918462811 scopus 로고    scopus 로고
    • This paper deals with racemic compounds. Only one of the enantiomers is shown.
  • 10
    • 0002149447 scopus 로고
    • Acid catalyzed ring opening of 3,4-epoxy-alkanols, review
    • (1980) Aldrichim. Acta , vol.13 , pp. 23
    • Kishi1
  • 11
    • 84918462810 scopus 로고    scopus 로고
    • In some cases, from stored solutions of epoxides of type 1 unstable carbamates of type 2 could be isolated; D. Hoppe, G. Tarara, unpublished work.
  • 13
    • 84918462809 scopus 로고    scopus 로고
    • max 45°). Further crystallographic details can be obtained on request from the Fachinformations= zentrum Energie Physik Mathematik, D-7514 Eggenstein-Leopoldshafen 2, FRG; please quote the full literature citation and the reference number CSD-51623.
  • 14
    • 84918462808 scopus 로고    scopus 로고
    • 3); 75.24 (C-2); 89.11 (C-4); 102.21 (C-1); 120.07, 128.98 and 136.57 (Aryl); 153.07 (C=O) ppm.
  • 18
    • 84918462807 scopus 로고    scopus 로고
    • 2,3 = 10.0 [7.5] Hz, J [[Truncated]]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.