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Volumn 7, Issue 6, 2001, Pages 1304-1308

Facial-selective allylation of methyl ketones for the asymmetric synthesis of α-substituted tertiary homoallylic ethers

Author keywords

Allylation; Amino alcohols; Homoallylic alcohols; Silanes

Indexed keywords

CATALYSIS; KETONES; SYNTHESIS (CHEMICAL);

EID: 0035896232     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20010316)7:6<1304::AID-CHEM1304>3.0.CO;2-9     Document Type: Article
Times cited : (28)

References (80)
  • 3
    • 0032859499 scopus 로고    scopus 로고
    • c) We recently described the enantioselective total synthesis of hydroxymyoporone using a facially selective allylation of an alkyl methyl ketone as the key step: L. F. Tietze, C. Wegner, C. Wulff, Chem. Eur. J. 1999, 5, 2885.
    • (1999) Chem. Eur. J. , vol.5 , pp. 2885
    • Tietze, L.F.1    Wegner, C.2    Wulff, C.3
  • 71
    • 0005619944 scopus 로고    scopus 로고
    • note
    • 13C NMR spectra.
  • 72
    • 0005640894 scopus 로고    scopus 로고
    • note
    • Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Center as supplementary publication no. CCDC-151421 (11), CCDC-151422 (12a) and CCDC-151423 (12c). Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK (fax: (+44) 1223-336-033; e-mail: deposit@ccdc.cam.ac.uk). The two stereogenic centres of the norpseudoephedrine moiety are known, therefore a heavy atom in the molecule is not necessary to calculate the absolute configuration.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.