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Volumn 86, Issue 10, 2008, Pages 970-975

Radical addition to ynol ethers - A convenient procedure for the stereoselective preparation of α-iodo enol ethers in neutral conditions

Author keywords

Enol ethers; Radical addition; Stereoselective; Ynol ethers

Indexed keywords

ETHERS; IODINE; REACTION KINETICS; STEREOSELECTIVITY;

EID: 50949097771     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/V08-094     Document Type: Article
Times cited : (6)

References (32)
  • 2
  • 5
    • 0028041228 scopus 로고    scopus 로고
    • For examples of cross coupling reactions involving α-halo enol ethers: (a) R.W. Friesen, R.W. Loo, and C.F. Sturino. Can. J. Chem. 72, 1262 (1994);
    • For examples of cross coupling reactions involving α-halo enol ethers: (a) R.W. Friesen, R.W. Loo, and C.F. Sturino. Can. J. Chem. 72, 1262 (1994);
  • 11
    • 0037223535 scopus 로고    scopus 로고
    • For preparation of α-halo enol ethers via stannyl intermediates
    • (c) S.F. Martin. Pure Appl. Chem. 75, 63 (2003). For preparation of α-halo enol ethers via stannyl intermediates:
    • (2003) Pure Appl. Chem , vol.75 , pp. 63
    • Martin, S.F.1
  • 18
    • 54549106297 scopus 로고    scopus 로고
    • Y. Amiel. In The chemistry of functional groups. Supplement C, The chemistry of triple bonded functional groups. Part I. Edited by S. Patai and Z. Rappoport. Wiley, Chichester. 1983. pp. 345-347;
    • (e) Y. Amiel. In The chemistry of functional groups. Supplement C, The chemistry of triple bonded functional groups. Part I. Edited by S. Patai and Z. Rappoport. Wiley, Chichester. 1983. pp. 345-347;
  • 20
    • 0042863663 scopus 로고    scopus 로고
    • Radical 4 is expected to interconvert very slowly since it is known that a-oxy vinyl radicals possess a very high energy barrier to rotation; see: (a) J.A. Kampmeier, M.S. Liu, S. Soloway, and D.K. Wedegaertner. J. Am. Chem. Soc. 93, 3809 (1971);
    • Radical 4 is expected to interconvert very slowly since it is known that a-oxy vinyl radicals possess a very high energy barrier to rotation; see: (a) J.A. Kampmeier, M.S. Liu, S. Soloway, and D.K. Wedegaertner. J. Am. Chem. Soc. 93, 3809 (1971);
  • 27
    • 0345635644 scopus 로고
    • For other methods for preparing β,β-dialkylated α-iodo enol ethers, see: a
    • For other methods for preparing β,β-dialkylated α-iodo enol ethers, see: (a) H.R. Sonawane, B.S. Nanjundiah, and M.D. Panse. Tetrahedron Lett. 26, 3507 (1985);
    • (1985) Tetrahedron Lett , vol.26 , pp. 3507
    • Sonawane, H.R.1    Nanjundiah, B.S.2    Panse, M.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.