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Volumn 131, Issue 45, 2009, Pages 16525-16528

C-H bond functionalization via hydride transfer: Direct coupling of unactivated alkynes and sp3 C-H bonds catalyzed by platinum tetraiodide

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYLATION; C-C BOND FORMATION; C-H BOND; CYCLIC ETHER; DIRECT COUPLING; FUNCTIONALIZATIONS; HALIDE LIGAND; HETEROCYCLIC COMPOUND; HYDRIDE TRANSFERS; INTRAMOLECULAR COUPLING; LEWIS ACID CATALYSTS; TERMINAL ALKYNE;

EID: 70450161823     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja906480w     Document Type: Article
Times cited : (161)

References (32)
  • 8
    • 58149293587 scopus 로고    scopus 로고
    • For other recent developments in the area of HT-cyclization, see
    • For other recent developments in the area of HT-cyclization, see: (a) Zhang, C.; Murarka, S.; Seidel, D. J. Org. Chem. 2009, 74, 419.
    • (2009) J. Org. Chem. , vol.74 , pp. 419
    • Zhang, C.1    Murarka, S.2    Seidel, D.3
  • 16
    • 70349783659 scopus 로고    scopus 로고
    • A related process with substituted alkynes
    • A related process with substituted alkynes: Yang, S.; Li, Z.; Jian, X.; He, C. Angew. Chem., Int. Ed. 2009, 48, 3999.
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 3999
    • Yang, S.1    Li, Z.2    Jian, X.3    He, C.4
  • 17
    • 67650551471 scopus 로고    scopus 로고
    • During review of this paper, the following report was published that describes an intramolecular coupling of terminal alkynes and amineoxides to afford piperidin-4-ones
    • During review of this paper, the following report was published that describes an intramolecular coupling of terminal alkynes and amineoxides to afford piperidin-4-ones. Cui, L.; Peng, Y.; Zhang, L. J. Am. Chem. Soc. 2009, 131, 8394.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 8394
    • Cui, L.1    Peng, Y.2    Zhang, L.3
  • 25
    • 70450142407 scopus 로고    scopus 로고
    • note
    • We have examined a broad array of metal complexes in the early stages of this project, including Rh(I) complexes, but only platinum salts provided practical yields of the desired products.
  • 26
    • 0032569211 scopus 로고    scopus 로고
    • Several reports noted that platinum bromides or iodides were better catalysts than platinum chlorides in the activation of alkynes for attack by carbon and heteroatom nucleophiles
    • Several reports noted that platinum bromides or iodides were better catalysts than platinum chlorides in the activation of alkynes for attack by carbon and heteroatom nucleophiles. (a) Fürstner, A.; Szillat, H.; Gabor, B.; Mynott, R. J. Am. Chem. Soc. 1998, 120, 8305.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 8305
    • Fürstner, A.1    Szillat, H.2    Gabor, B.3    Mynott, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.