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Volumn 1, Issue 6, 2011, Pages 601-606

Cationic gold catalyzes ω-bromination of terminal alkynes and subsequent hydroaddition reactions

Author keywords

, bisfunctionalization; aurophilic interactions; bromoalkynes; gold catalysis; terminal alkynes

Indexed keywords

AUROPHILIC INTERACTION; BROMOALKYNES; C-H BOND; CATALYTIC AMOUNTS; CATIONIC GOLD; GOLD CATALYSIS; NUCLEOPHILIC ATTACK; TERMINAL ALKYNE; TERMINAL ALKYNES;

EID: 79958232389     PISSN: 21555435     EISSN: None     Source Type: Journal    
DOI: 10.1021/cs200168p     Document Type: Article
Times cited : (35)

References (70)
  • 7
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    • For a very recent review on isolated intermediates see
    • For a very recent review on isolated intermediates see: Hashmi, A. S. K. Angew. Chem., Int. Ed. 2010, 49, 5232
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 5232
    • Hashmi, A.S.K.1
  • 28
    • 0038252959 scopus 로고    scopus 로고
    • This chemical behavior resembles that of zinc in Carreira's system, for a review see
    • This chemical behavior resembles that of zinc in Carreira's system, for a review see: Frantz, D. E.; Fässler, R.; Tomooka, C. S.; Carreira, E. M. Acc. Chem. Res. 2000, 33, 373
    • (2000) Acc. Chem. Res. , vol.33 , pp. 373
    • Frantz, D.E.1    Fässler, R.2    Tomooka, C.S.3    Carreira, E.M.4
  • 31
    • 77949599382 scopus 로고    scopus 로고
    • Compound 6c is indeed a mixture of compounds as assessed by XRD studies
    • Hooper, T. N.; Green, M.; Russell, C. A. Chem. Commun. 2010, 46, 2313; Compound 6c is indeed a mixture of compounds as assessed by XRD studies
    • (2010) Chem. Commun. , vol.46 , pp. 2313
    • Hooper, T.N.1    Green, M.2    Russell, C.A.3
  • 37
    • 51049119035 scopus 로고    scopus 로고
    • If an intramolecular electrophile is present, after π-coordination the cycloisomerisation outruns the protodeauration, see
    • If an intramolecular electrophile is present, after π-coordination the cycloisomerisation outruns the protodeauration, see: Hashmi, A. S. K.; Rudolph, M.; Siehl, H-. U.; Tanaka, M.; Bats, J. W.; Frey, W. Chem. - Eur. J. 2008, 14, 3703
    • (2008) Chem. - Eur. J. , vol.14 , pp. 3703
    • Hashmi, A.S.K.1    Rudolph, M.2    Siehl, H.U.3    Tanaka, M.4    Bats, J.W.5    Frey, W.6
  • 46
    • 77953630250 scopus 로고    scopus 로고
    • Reaction of gold intermediates with NIS is well-precedented, see:;;, and also refs 47-49
    • Reaction of gold intermediates with NIS is well-precedented, see: Sethofer, S. G.; Mayer, T.; Toste, F. D. J. Am. Chem. Soc. 2010, 132, 8276, and also refs 47-49
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 8276
    • Sethofer, S.G.1    Mayer, T.2    Toste, F.D.3
  • 53
    • 77956930222 scopus 로고    scopus 로고
    • Use of NIS for the oxidative addition to Au(I) has been reported, see
    • Use of NIS for the oxidative addition to Au(I) has been reported, see: Scott, V. J.; Labinger, J. A.; Bercaw, J. E. Organometallics 2010, 29, 4090
    • (2010) Organometallics , vol.29 , pp. 4090
    • Scott, V.J.1    Labinger, J.A.2    Bercaw, J.E.3
  • 54
    • 78149425384 scopus 로고    scopus 로고
    • Formation of diaurated species should not be ruled out, see
    • Formation of diaurated species should not be ruled out, see: Seidel, G.; Lehmann, C. W.; Fürstner, A. Angew. Chem., Int. Ed. 2010, 49, 8466
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 8466
    • Seidel, G.1    Lehmann, C.W.2    Fürstner, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.