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Volumn 30, Issue 9, 2011, Pages 2598-2608

Protecting-group-free access to a three-coordinate nickel(0) tris-isocyanide

Author keywords

[No Author keywords available]

Indexed keywords

FREE ACCESS; ISOCYANIDES; LEWIS ACID; LEWIS BASE; OXIDATIVE ADDITION REACTION; PROTECTION STRATEGY; TERPHENYLS; TETRAKIS;

EID: 79955623622     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om200209w     Document Type: Article
Times cited : (54)

References (99)
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    • 3 using the ADF 2007.01 program suite. Full details are presented in the Supporting Information.
    • 3 using the ADF 2007.01 program suite. Full details are presented in the Supporting Information.
  • 42
    • 79955596006 scopus 로고    scopus 로고
    • note
    • Dipp2 resonances, thus suggesting that fast ligand exchange processes do not take place (see the Supporting Information).
  • 47
    • 79955578658 scopus 로고    scopus 로고
    • note
    • 2 will be reported in a subsequent publication.
  • 48
    • 0000331994 scopus 로고
    • Dipp2 functioning as a strong σ-donor to a weakly π-basic divalent Ni center. See ref 30 and Robertson, M. J.; Angelici, R. J. Langmuir 1994, 10, 1488-1492
    • (1994) Langmuir , vol.10 , pp. 1488-1492
    • Robertson, M.J.1    Angelici, R.J.2
  • 52
    • 79955610956 scopus 로고    scopus 로고
    • See the Supporting Information for experimental details.
    • See the Supporting Information for experimental details.
  • 53
    • 79955637549 scopus 로고    scopus 로고
    • 3.
    • 3.
  • 83
    • 79955573295 scopus 로고    scopus 로고
    • Conversion (%) to product relative to aryl halide starting material (average of two runs): p -chlorotoluene = 3%; mesityl bromide 14%. See the Experimental Section for full details on reaction conditions.
    • Conversion (%) to product relative to aryl halide starting material (average of two runs): p -chlorotoluene = 3%; mesityl bromide 14%. See the Experimental Section for full details on reaction conditions.
  • 85
    • 3042734823 scopus 로고    scopus 로고
    • For studies detailing the electronic structure and reactivity of Ni complexes in catalytic cross-coupling, in addition to the role of strong-field ligands and additives in catalysis, see
    • For studies detailing the electronic structure and reactivity of Ni complexes in catalytic cross-coupling, in addition to the role of strong-field ligands and additives in catalysis, see: Anderson, T. J.; Jones, G. D.; Vicic, D. A. J. Am. Chem. Soc. 2004, 126, 8100-8101
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 8100-8101
    • Anderson, T.J.1    Jones, G.D.2    Vicic, D.A.3
  • 92
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    • SCM, Theoretical Chemistry, Vrije Universiteit: Amsterdam, The Netherlands;. Access date: October.
    • ADF 2007.01; SCM, Theoretical Chemistry, Vrije Universiteit: Amsterdam, The Netherlands; www.scm.com. Access date: October 2007.
    • (2007) ADF 2007.01
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    • erratum.
    • Perdew, J. P. Phys. Rev. B 1986, 34, 7406-7406; erratum.
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    • SCM: Amsterdam, The Netherlands;. Access date: Nov.
    • ADF-GUI 2009.01; SCM: Amsterdam, The Netherlands; www.scm.com. Access date: Nov 2009.
    • (2009) ADF-GUI 2009.01


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.