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Volumn 71, Issue 14, 2006, Pages 5384-5387

A SeCSe-Pd(II) pincer complex as a highly efficient catalyst for allylation of aldehydes with allyltributyltin

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; AROMATIC COMPOUNDS; CARBON; CATALYSTS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PALLADIUM; SELENIUM; SYNTHESIS (CHEMICAL); THERMAL EFFECTS;

EID: 33745714345     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo060456k     Document Type: Article
Times cited : (59)

References (43)
  • 4
    • 0002446724 scopus 로고
    • Heathcock, C. H., Ed.; Pergamon Press: Oxford
    • (c) Roush, W. R. In Comprehensive Organic Synthesis; Heathcock, C. H., Ed.; Pergamon Press: Oxford, 1991; Vol. 2, pp 1-53.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 1-53
    • Roush, W.R.1
  • 6
    • 0002026625 scopus 로고    scopus 로고
    • Otera, J., Ed.; Wiley-VHC: Weinheim, Germany, Chapter 11
    • (e) Chemler, S. R.; Roush, R. W. In Modern Carbonyl Chemistry; Otera, J., Ed.; Wiley-VHC: Weinheim, Germany, 2000; Chapter 11.
    • (2000) Modern Carbonyl Chemistry
    • Chemler, S.R.1    Roush, R.W.2
  • 9
    • 0004063249 scopus 로고    scopus 로고
    • Wiley-VCH: Weinheim, Germany, Chapter 5
    • (c) Davies. A. G. Organotin Chemistry; Wiley-VCH: Weinheim, Germany, 2004; Chapter 5.
    • (2004) Organotin Chemistry
    • Davies, A.G.1
  • 19
    • 0041878778 scopus 로고    scopus 로고
    • For an excellent recent review, see: Denmark, S. E.; Fu, J. Chem. Rev. 2003, 103, 2763.
    • (2003) Chem. Rev. , vol.103 , pp. 2763
    • Denmark, S.E.1    Fu, J.2
  • 23
    • 0029929193 scopus 로고    scopus 로고
    • (b) Nakamura, H.; Iwama, H.; Yamamoto, Y. J. Am. Chem. Soc. 1996, 118, 6641. Simple Pd(II) or Pt(II) salts, such as PdCh and PtCb, catalyze the allylation of aldehydes with allyltributyltin with only poor yield; see ref 3a.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 6641
    • Nakamura, H.1    Iwama, H.2    Yamamoto, Y.3
  • 38
    • 33745708662 scopus 로고    scopus 로고
    • note
    • For a clarification of Lewis acid-catalyzed and Lewis acid-promoted reactions of allylstannanes, see ref 6b.
  • 39
    • 33745722796 scopus 로고    scopus 로고
    • note
    • The reaction was found to be very slow when a stoichiometric mixture of 4 and 7 was used in this NMR experiment.
  • 40
    • 33745708663 scopus 로고    scopus 로고
    • note
    • 8 at -5°C after 4 reacted with 7 for 20 min at 25°C. Details of this NMR study are given in the Supporting Information.
  • 41
    • 33745694571 scopus 로고    scopus 로고
    • note
    • The isolation, purification, and handling of catalyst 4 are all performed in open vessels under ambient conditions without special precautions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.