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Volumn 48, Issue 10, 2007, Pages 1761-1765

Copper(I) iodide dimethyl sulfide catalyzed 1,4-addition of alkenyl groups from alkenyl-alkylzincate reagents

Author keywords

1,4 Addition; Conjugate addition; Copper catalyzed

Indexed keywords

ALKENYL GROUP; CARBONYL DERIVATIVE; COPPER DERIVATIVE; COPPER IODIDE DIMETHYLSULFIDE; DIMETHYL SULFIDE; IODINE DERIVATIVE; METHYL CHLORIDE; REAGENT; UNCLASSIFIED DRUG; VINYL DERIVATIVE; ZIRCONOCENE;

EID: 33846786810     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.01.041     Document Type: Article
Times cited : (6)

References (53)
  • 15
    • 0001252662 scopus 로고
    • An initial observation that CuOTf facilitate the 1,4-addition of vinylgroups, see: Ref. 1a
    • Loots M.J., and Schwartz J. J. Am. Chem. Soc. 99 (1977) 8045-8046 An initial observation that CuOTf facilitate the 1,4-addition of vinylgroups, see: Ref. 1a
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 8045-8046
    • Loots, M.J.1    Schwartz, J.2
  • 35
    • 33846799785 scopus 로고    scopus 로고
    • note
    • 2Zn can also be employed.
  • 36
    • 33846806411 scopus 로고    scopus 로고
    • note
    • For experimental details, see: Supplementary data.
  • 37
    • 0028806823 scopus 로고
    • The CuI·DMS complex is unstable and loses DMS rapidly to form the more stable CuI·0.75DMS stoichiometry, as determined by elemental analysis. For a discussion on the stability of CuI·DMS complex, see:
    • The CuI·DMS complex is unstable and loses DMS rapidly to form the more stable CuI·0.75DMS stoichiometry, as determined by elemental analysis. For a discussion on the stability of CuI·DMS complex, see:. Eriksson M., Hjelmencrantz A., Nilsson M., and Olsson T. Tetrahedron 51 (1995) 12631-12644
    • (1995) Tetrahedron , vol.51 , pp. 12631-12644
    • Eriksson, M.1    Hjelmencrantz, A.2    Nilsson, M.3    Olsson, T.4
  • 39
    • 0001264816 scopus 로고
    • CuI purified via its dimethyl sulfide complex, see:
    • CuI purified via its dimethyl sulfide complex, see:. House H.O., Chu C.-Y., Wilkins J.M., and Umen M.J. J. Org. Chem. 40 (1975) 1460-1469
    • (1975) J. Org. Chem. , vol.40 , pp. 1460-1469
    • House, H.O.1    Chu, C.-Y.2    Wilkins, J.M.3    Umen, M.J.4
  • 41
    • 33846812021 scopus 로고    scopus 로고
    • note
    • 2 promoted 1,4-additions, see Ref. 15.
  • 46
    • 33846809781 scopus 로고    scopus 로고
    • note
    • 1H NMR reveals opening of the oxazolidinone ring.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.