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Volumn 131, Issue 9, 2009, Pages 3166-3167

Rh-catalyzed isomerization and intramolecular redox reaction of alkynyl ethers affording dihydropyrans and ketoolefins

Author keywords

[No Author keywords available]

Indexed keywords

DEUTERIUM; ETHERS; REDOX REACTIONS; RHODIUM; TOLUENE;

EID: 67749142078     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja809826a     Document Type: Article
Times cited : (123)

References (37)
  • 10
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    • For recent reviews on C-H bond activation, see: a
    • For recent reviews on C-H bond activation, see: (a) Alberico, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007, 107, 174-238.
    • (2007) Chem. Rev. , vol.107 , pp. 174-238
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 11
    • 33947493717 scopus 로고    scopus 로고
    • (b) Bergman, R. G Nature 2007, 446, 391-393.
    • (2007) Nature , vol.446 , pp. 391-393
    • Bergman, R.G.1
  • 19
    • 54749149062 scopus 로고    scopus 로고
    • Latest reports on transition metal mediated α-ether C-H bond activation are as follows. With Fe: a, With Rh
    • Latest reports on transition metal mediated α-ether C-H bond activation are as follows. With Fe: (a) Li, Z.; Yu, R.; Li, H. Angew. Chem., Int. Ed. 2008, 47, 7497-7500. With Rh
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 7497-7500
    • Li, Z.1    Yu, R.2    Li, H.3
  • 22
    • 30744436813 scopus 로고    scopus 로고
    • This observation should be useful for the preparation of polysubstituted sixmembered oxacycles, which are often found in naturally occurring products. For reviews, see: a, Gladysz, J. A., Ed, For a review on their preparative methods, see
    • This observation should be useful for the preparation of polysubstituted sixmembered oxacycles, which are often found in naturally occurring products. For reviews, see: (a) Gladysz, J. A., Ed. Chem. Rev. 2005, 105, 4235-4807. For a review on their preparative methods, see
    • (2005) Chem. Rev. , vol.105 , pp. 4235-4807
  • 23
    • 33646403425 scopus 로고    scopus 로고
    • For representative natural cis-2-alkyl-6-aryltetrahydropyrans, see
    • (b) Clarke, P. A.; Santos, S. Eur. J. Org. Chem. 2006, 2045-2054. For representative natural cis-2-alkyl-6-aryltetrahydropyrans, see
    • (2006) Eur. J. Org. Chem. , pp. 2045-2054
    • Clarke, P.A.1    Santos, S.2
  • 31
    • 35348824909 scopus 로고    scopus 로고
    • For a review on activation of olefins and acetylenes with transition metal species, see
    • For a review on activation of olefins and acetylenes with transition metal species, see: Yamamoto, Y. J. Org. Chem. 2007, 72, 7817-7831.
    • (2007) J. Org. Chem. , vol.72 , pp. 7817-7831
    • Yamamoto, Y.1
  • 32
    • 28844500714 scopus 로고    scopus 로고
    • Cyclization of carbonyl and α, β-unsaturated carbonyl compounds via Lewis acid mediated C-H bond activation was reported recently
    • Cyclization of carbonyl and α, β-unsaturated carbonyl compounds via Lewis acid mediated C-H bond activation was reported recently: Pastine, S. J.; Sames, D. Org. Lett. 2005, 7, 5429-5431.
    • (2005) Org. Lett. , vol.7 , pp. 5429-5431
    • Pastine, S.J.1    Sames, D.2
  • 34
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    • For intramolecular redox reaction from propargyl alcohols to α, β-olefinic carbonyl compounds, see: a, and references cited therein
    • For intramolecular redox reaction from propargyl alcohols to α, β-olefinic carbonyl compounds, see: (a) Trost, B. M.; Livingston, R. C. J. Am. Chem. Soc. 2008, 130, 11970-11978, and references cited therein.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11970-11978
    • Trost, B.M.1    Livingston, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.