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Volumn 130, Issue 3, 2008, Pages 802-803

Efficient control of π-alkyne and vinylidene complex pathways for the W(CO)5(L)-catalyzed synthesis of two types of nitrogen-containing bicyclic compounds

Author keywords

[No Author keywords available]

Indexed keywords

2 AZABICYCLO[3.3.0]OCTANE; 3 AZABICYCLO[3.3.0]OCTANE; ALKYNE; AMINE; BICYCLO COMPOUND; BICYCLO[3.3.0]OCTANE DERIVATIVE; CARBENE; CARBON; CARBON 13; DEUTERIUM; METAL COMPLEX; NITROGEN DERIVATIVE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 38349130836     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0782605     Document Type: Article
Times cited : (29)

References (29)
  • 1
    • 34250824768 scopus 로고    scopus 로고
    • For recent reviews of electrophilic activation of alkynes, see; a
    • For recent reviews of electrophilic activation of alkynes, see; (a) Fürstner, A.; Davies, P. W. Angew. Chem., Int. Ed. 2007, 46, 3410.
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 3410
    • Fürstner, A.1    Davies, P.W.2
  • 6
    • 35348824909 scopus 로고    scopus 로고
    • For recent reviews of electrophilic activation of alkynes by using other transiton-metal complexes, a
    • For recent reviews of electrophilic activation of alkynes by using other transiton-metal complexes, (a) Yamamoto, Y. J. Org. Chem. 2007, 72, 7817.
    • (2007) J. Org. Chem , vol.72 , pp. 7817
    • Yamamoto, Y.1
  • 9
    • 5244284889 scopus 로고
    • For reviews on metal vinylidene chemistry, see: a
    • For reviews on metal vinylidene chemistry, see: (a) Bruce, M. I. Chem. Rev. 1991, 91, 197.
    • (1991) Chem. Rev , vol.91 , pp. 197
    • Bruce, M.I.1
  • 12
    • 33745777313 scopus 로고    scopus 로고
    • For recent reviews on the catalytic C-C bond formations utilizing vinylidene complex as a key intermediate, see: (a) Bruneau, C, Dixneuf, P. H. Angew. Chem, Int. Ed. 2006, 45, 2176
    • For recent reviews on the catalytic C-C bond formations utilizing vinylidene complex as a key intermediate, see: (a) Bruneau, C.; Dixneuf, P. H. Angew. Chem., Int. Ed. 2006, 45, 2176.
  • 16
    • 33846805830 scopus 로고    scopus 로고
    • For recent examples on the catalytic C-C bond formations utilizing vinylidene complex, see: a
    • For recent examples on the catalytic C-C bond formations utilizing vinylidene complex, see: (a) Kim, H.; Goble, S. D.; Lee, C. J. Am. Chem. Soc. 2007, 129, 1030.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 1030
    • Kim, H.1    Goble, S.D.2    Lee, C.3
  • 19
    • 0034801531 scopus 로고    scopus 로고
    • We have already succeeded in controlling π-alkyne- and vinylidene-complex pathways in the W(CO)5(L)-promoted reaction of o-ethynylphenyl ketone derivatives, but the reaction via vinylidene complex was stoichiometric: from π-alkyne complex, see: (a) Iwasawa, N, Shido, M, Kusama, H. J. Am. Chem. Soc. 2001, 123, 5814
    • 5(L)-promoted reaction of o-ethynylphenyl ketone derivatives, but the reaction via vinylidene complex was stoichiometric: from π-alkyne complex, see: (a) Iwasawa, N.; Shido, M.; Kusama, H. J. Am. Chem. Soc. 2001, 123, 5814.
  • 22
    • 26844464677 scopus 로고    scopus 로고
    • Ohe and Uemura also have reported the same control of π-alkyne- and vinylidene-complex pathways, see: d
    • Ohe and Uemura also have reported the same control of π-alkyne- and vinylidene-complex pathways, see: (d) Miki, K.; Uemura, S.; Ohe, K. Chem. Lett. 2005, 34, 1068.
    • (2005) Chem. Lett , vol.34 , pp. 1068
    • Miki, K.1    Uemura, S.2    Ohe, K.3
  • 26
  • 27
    • 7044241203 scopus 로고    scopus 로고
    • See also, ref 6e. (b) Alcázar, E.; Pletcher, J. M.; McDonald, F. E. Org. Lett. 2004, 6, 3877.
    • See also, ref 6e. (b) Alcázar, E.; Pletcher, J. M.; McDonald, F. E. Org. Lett. 2004, 6, 3877.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.