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Volumn 30, Issue 12, 2006, Pages 1844-1847

Corrections to a history of olefin metathesis

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; CYCLOBUTANE DERIVATIVE; NIOBIUM; TANTALUM; TUNGSTEN;

EID: 33846226049     PISSN: 11440546     EISSN: 13699261     Source Type: Journal    
DOI: 10.1039/b600533k     Document Type: Review
Times cited : (13)

References (63)
  • 5
    • 33644922320 scopus 로고    scopus 로고
    • R. H. Grubbs, Wiley-VCH, Weinheim
    • Handbook of Metathesis, ed., R. H. Grubbs,, Wiley-VCH, Weinheim, 2003, vols 1-3
    • (2003) Handbook of Metathesis, Ed. , vol.1-2
  • 8
    • 18944371935 scopus 로고    scopus 로고
    • Angew. Chem. 2005 117 3070
    • T. J. Katz Angew. Chem., Int. Ed. 2005 44 3010 Angew. Chem. 2005 117 3070
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 3010
    • Katz, T.J.1
  • 9
    • 0000025387 scopus 로고
    • For example, both the Royal Swedish Academy and C. P. Casey recommended the article for reading and incorporated portions of it in their writings.
    • T. J. Katz Adv. Organomet. Chem. 1977 16 283
    • (1977) Adv. Organomet. Chem. , vol.16 , pp. 283
    • Katz, T.J.1
  • 10
    • 33846227946 scopus 로고    scopus 로고
    • http://nobelprize.org/chemistry/laureates/2005/chemreading.html
  • 11
    • 33846185506 scopus 로고    scopus 로고
    • http://nobelprize.org/chemistry/laureates/2005/adv.html
  • 12
    • 31644447881 scopus 로고    scopus 로고
    • Others claim the article supports the research in their publications
    • C. P. Casey J. Chem. Educ. 2006 83 192
    • (2006) J. Chem. Educ. , vol.83 , pp. 192
    • Casey, C.P.1
  • 13
    • 33846249974 scopus 로고    scopus 로고
    • 1H NMR signals for the tert-butoxy groups, while structure 1 would exhibit only one.
    • A catalytic transformation cannot be unimolecular
  • 23
    • 33644922320 scopus 로고    scopus 로고
    • R. H. Grubbs, Wiley-VCH, Weinheim, ref. 3b Some have recognized that the synonyms cannot be distinguished:
    • T. J. Katz, in Handbook of Metathesis, ed., R. H. Grubbs,, Wiley-VCH, Weinheim, 2003, vol. 1, ch. 1.5
    • (2003) Handbook of Metathesis, Ed.
    • Katz In, T.J.1
  • 29
    • 33846215520 scopus 로고    scopus 로고
    • 4
    • 4
  • 31
    • 33846235902 scopus 로고
    • Ger. Pat. 1,072,811
    • H. S. Eleuterio, Ger. Pat. 1,072,811, 1960
    • (1960)
    • Eleuterio, H.S.1
  • 36
    • 58149326227 scopus 로고
    • reported that a not fully specified Schrock tungsten-carbene converts cyclooctene in unspecified yield into 90%-cis-polyoctenamer and cyclopentene, cyclodecene, and cyclododecene into 55-, 20-, and 20%-cis-polyalkenamers. Cycloheptene gives no polymer. Schrock molybdenum-carbenes give polymers whose double bonds are mainly trans Norbornene derivatives have sometimes given high stereoselectivities.
    • P. Dounis W. J. Feast A. M. Kenwright Polymer 1995 36 2787
    • (1995) Polymer , vol.36 , pp. 2787
    • Dounis, P.1    Feast, W.J.2    Kenwright, A.M.3
  • 41
    • 33846199542 scopus 로고    scopus 로고
    • R. H. Grubbs, Wiley-VCH, Weinheim, 3, ch. 3.5, and references therein
    • J. G. Hamilton, in Handbook of Metathesis, ed., R. H. Grubbs,, Wiley-VCH, Weinheim, 2003, vol. 3, ch. 3.5
    • (2003) Handbook of Metathesis, Ed.
    • Hamilton In, J.G.1
  • 48
    • 33846263639 scopus 로고    scopus 로고
    • See also:
    • See also: http://www.columbia.edu/cu/chemistry/fac-bios/katz/group/pages/ publications.html#N10478
  • 49
    • 33846240021 scopus 로고    scopus 로고
    • 6, and 0.6% based on 2-butene
    • 6, and 0.6% based on 2-butene
  • 51
    • 33846217401 scopus 로고
    • 4Sn, see: Ger. Pat. DE1909951
    • 4Sn, see: C. P. C. Bradshaw, Ger. Pat. DE1909951, 1969
    • (1969)
    • Bradshaw, C.P.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.