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Volumn 327, Issue 5963, 2010, Pages 315-319

Ligand-enabled reactivity and selectivity in a synthetically versatile Aryl C-H olefination

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE; CARBON; CARBOXYLIC ACID; HYDROCINNAMIC ACID; LIGAND; NAPHTHALENE DERIVATIVE; NATURAL PRODUCT; OXIDIZING AGENT; OXYGEN; PALLADIUM; PHENYLACETIC ACID; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; TETRALIN DERIVATIVE;

EID: 74549148904     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1182512     Document Type: Article
Times cited : (658)

References (37)
  • 20
    • 74549216467 scopus 로고    scopus 로고
    • For early examples of Pd-catalyzed directed and nondirected arene C-H olefination, see (31-33). For an early example of Ru-catalyzed directed olefination, see (34)
    • For early examples of Pd-catalyzed directed and nondirected arene C-H olefination, see (31-33). For an early example of Ru-catalyzed directed olefination, see (34).
  • 24
    • 74549120270 scopus 로고    scopus 로고
    • For application of mono-N-protected amino acid ligands for Pd-catalyzed enantioselective C-H activation/C-C cross coupling, see 35
    • For application of mono-N-protected amino acid ligands for Pd-catalyzed enantioselective C-H activation/C-C cross coupling, see (35).
  • 30
    • 74549181360 scopus 로고    scopus 로고
    • For discussion of the importance of ligand development in Pd chemistry, see 36
    • For discussion of the importance of ligand development in Pd chemistry, see (36).
  • 32
    • 0034677867 scopus 로고
    • C. G. Jia et al., Science 287, 1992 (2000).
    • (1992) Science , vol.287 , pp. 2000
    • Jia, C.G.1
  • 34
    • 0027913099 scopus 로고
    • S. Murai et al., Nature 366, 529 (1993).
    • (1993) Nature , vol.366 , pp. 529
    • Murai, S.1
  • 37
    • 74549188454 scopus 로고    scopus 로고
    • Supported by an A. P. Sloan Foundation fellowship (J.-Q.Y.); predoctoral fellowships from NSF, the U.S. Department of Defense, the Scripps Research Institute, and the Skaggs Oxford Scholarship program (K.M.E.); and the Scripps Research Institute, National Institute of General Medical Sciences grant 1 RO1 GM084019-02, NSF grant CHE-0910014, Amgen, and Eli Lilly & Co.
    • Supported by an A. P. Sloan Foundation fellowship (J.-Q.Y.); predoctoral fellowships from NSF, the U.S. Department of Defense, the Scripps Research Institute, and the Skaggs Oxford Scholarship program (K.M.E.); and the Scripps Research Institute, National Institute of General Medical Sciences grant 1 RO1 GM084019-02, NSF grant CHE-0910014, Amgen, and Eli Lilly & Co.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.