메뉴 건너뛰기




Volumn 25, Issue 5, 2006, Pages 1217-1229

Palladium-catalyzed pathways to aryl-substituted indenes: Efficient synthesis of ligands and the respective ansa-zirconocenes

Author keywords

[No Author keywords available]

Indexed keywords

MOLECULAR STRUCTURE; OLEFINS; PALLADIUM; SYNTHESIS (CHEMICAL); ZIRCONIUM COMPOUNDS;

EID: 33644923489     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om050937e     Document Type: Article
Times cited : (50)

References (133)
  • 4
    • 0004032979 scopus 로고    scopus 로고
    • Togni, A., Halterman, R. L., Eds.; Wiley-VCH: Weinheim, Germany, and references therein
    • (d) Metallocenes: Synthesis, Reactivity, Applications; Togni, A., Halterman, R. L., Eds.; Wiley-VCH: Weinheim, Germany, 1998, and references therein.
    • (1998) Metallocenes: Synthesis, Reactivity, Applications
  • 18
    • 33644905607 scopus 로고    scopus 로고
    • U.S. Patent 5,965,759 for Albemarle Corp.
    • Lin, R. W. U.S. Patent 5,965,759 for Albemarle Corp., 1999.
    • (1999)
    • Lin, R.W.1
  • 23
    • 33644880574 scopus 로고    scopus 로고
    • U.S. Patent 5,789,634 for Boulder Scientific Co.
    • (c) Sullivan, J. M.; Barnes, H. H. U.S. Patent 5,789,634 for Boulder Scientific Co., 1998.
    • (1998)
    • Sullivan, J.M.1    Barnes, H.H.2
  • 58
    • 0013150721 scopus 로고    scopus 로고
    • Schlosser, M., Ed.; Wiley-VCH: Weinheim, Germany, and references therein
    • (a) Schlosser, M. In Organometallics in Synthesis: A Manual; Schlosser, M., Ed.; Wiley-VCH: Weinheim, Germany, 2002; pp 1-352, and references therein.
    • (2002) Organometallics in Synthesis: A Manual , pp. 1-352
    • Schlosser, M.1
  • 79
    • 0000975959 scopus 로고    scopus 로고
    • Liebeskind, L. S., Ed.; JAI: Amsterdam
    • (g) Miyaura, N. In Advances in Metal-organic Chemistry; Liebeskind, L. S., Ed.; JAI: Amsterdam, 1998; Vol. 6, pp 187-243.
    • (1998) Advances in Metal-organic Chemistry , vol.6 , pp. 187-243
    • Miyaura, N.1
  • 80
    • 0001786881 scopus 로고    scopus 로고
    • Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany
    • (h) Suzuki, A. In Metal-catalyzed Cross-coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1998; pp 49-89.
    • (1998) Metal-catalyzed Cross-coupling Reactions , pp. 49-89
    • Suzuki, A.1
  • 82
    • 0011476461 scopus 로고    scopus 로고
    • ACS Symposium Series 783; Ramachandran, P. V., Brown, H. C., Eds.; American Chemical Society: Washington, DC
    • (j) Suzuki, A. In Organoboranes for Synthesis; ACS Symposium Series 783; Ramachandran, P. V., Brown, H. C., Eds.; American Chemical Society: Washington, DC, 2001; pp 80-93.
    • (2001) Organoboranes for Synthesis , pp. 80-93
    • Suzuki, A.1
  • 99
    • 0034812321 scopus 로고    scopus 로고
    • 3 are as follows, (a) Negishi reaction: Dai, C.; Fu, G. C. J. Am. Chem. Soc. 2001, 123, 2719.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 2719
    • Dai, C.1    Fu, G.C.2
  • 107
    • 0002521096 scopus 로고    scopus 로고
    • Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany
    • Negishi, E.; Liu, F. In Metal-catalyzed Cross-coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1998; pp 1-47.
    • (1998) Metal-catalyzed Cross-coupling Reactions , pp. 1-47
    • Negishi, E.1    Liu, F.2
  • 108
    • 0004194357 scopus 로고    scopus 로고
    • Knochel, P., Jones, P., Eds.; Oxford University Press: London, and references therein
    • Negishi, E. In Organozinc reagents. A Practical Approach; Knochel, P., Jones, P., Eds.; Oxford University Press: London, 1999; pp 213-243, and references therein.
    • (1999) Organozinc Reagents. A Practical Approach , pp. 213-243
    • Negishi, E.1
  • 110
    • 0000725544 scopus 로고    scopus 로고
    • Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, and references therein
    • (b) Mitchell, T. N. In Metal-catalyzed Cross-coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1998; pp 167-197, and references therein.
    • (1998) Metal-catalyzed Cross-coupling Reactions , pp. 167-197
    • Mitchell, T.N.1
  • 111
    • 33644887205 scopus 로고    scopus 로고
    • note
    • 2PCl followed by treatment of the reaction mixture with aqueous HCl. In this way, indene 36 has been obtained in 87% yield.
  • 112
    • 33644881697 scopus 로고    scopus 로고
    • note
    • 11b
  • 131
    • 33644896015 scopus 로고    scopus 로고
    • All experimental details can be found in the Supporting Information
    • All experimental details can be found in the Supporting Information.
  • 132
    • 0347111342 scopus 로고    scopus 로고
    • Bruker/Siemens Area Detector Absorption Correction Program; Bruker AXS, Madison, WI
    • Sheldrick G. M. SADABS, V2.01, Bruker/Siemens Area Detector Absorption Correction Program; Bruker AXS, Madison, WI, 1998.
    • (1998) SADABS, V2.01
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.