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Volumn 60, Issue 34, 2004, Pages 7431-7437

Regioselectivity in nickel(0) catalyzed cycloadditions of carbon dioxide with diynes

Author keywords

Carbon dioxide; Cycloaddition; N heterocyclic carbenes; Nickel; Regioselectivities

Indexed keywords

ALKENE DERIVATIVE; CARBENE; CARBON DIOXIDE; METHYL GROUP; NICKEL; PYRONE DERIVATIVE;

EID: 3342989847     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.06.025     Document Type: Conference Paper
Times cited : (130)

References (29)
  • 19
    • 0000186209 scopus 로고
    • The data provided from Tsuda does not unambiguously establish the regiochemistry of the pyrone product obtained from the cycloaddition of diyne
    • The data provided from Tsuda does not unambiguously establish the regiochemistry of the pyrone product obtained from the cycloaddition of diyne 14. See ref: Tsuda T., Morikawa S., Hasegawa N., Saegusa T. J. Org. Chem. 55:1990;2978
    • (1990) J. Org. Chem. , vol.55 , pp. 2978
    • Tsuda, T.1    Morikawa, S.2    Hasegawa, N.3    Saegusa, T.4
  • 20
    • 4043118703 scopus 로고    scopus 로고
    • A corrigendum has recently been submitted to J. Am. Chem. Soc.
    • A corrigendum has recently been submitted to J. Am. Chem. Soc.
  • 21
    • 33845279846 scopus 로고
    • For an in-depth discussion of cyclotrimer side-product formation, see
    • For an in-depth discussion of cyclotrimer side-product formation, see Tsuda T., Morikawa S., Sumiya R., Saegusa T. J. Org. Chem. 53:1988;3140
    • (1988) J. Org. Chem. , vol.53 , pp. 3140
    • Tsuda, T.1    Morikawa, S.2    Sumiya, R.3    Saegusa, T.4
  • 22
    • 4043160955 scopus 로고    scopus 로고
    • note
    • In the cycloaddition reaction with substrate 3, a cyclotrimerized aromatic product was isolated in 18% yield. However, in reactions that typically afforded a mixture of products, the oligomers were not isolated
  • 25
    • 1842607439 scopus 로고    scopus 로고
    • This is a rare example where the formation of a carbon-carbon bond adjacent to the sterically more hindered side of an alkyne is favored. For other examples, see Ref. 7 and
    • This is a rare example where the formation of a carbon-carbon bond adjacent to the sterically more hindered side of an alkyne is favored. For other examples, see Ref. 7 and Miller K.M., Luanphaisarnnont T., Molinaro C., Jamison T.F. J. Am. Chem. Soc. 126:2004;4130
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4130
    • Miller, K.M.1    Luanphaisarnnont, T.2    Molinaro, C.3    Jamison, T.F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.