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Volumn 50, Issue 25, 2011, Pages 5658-5661

Terminating platinum-initiated cation-olefin reactions with simple alkenes

Author keywords

biomimetic synthesis; cascade cyclization; electrophilic activation; platinum

Indexed keywords

BIOMIMETIC SYNTHESIS; CASCADE CYCLIZATION; CYCLASES; CYCLIZATIONS; ELECTROPHILES; ELECTROPHILIC ACTIVATION; POLYALKENES; TERMINAL ALKENES; TERMINATING GROUPS;

EID: 79958260968     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201100463     Document Type: Article
Times cited : (39)

References (49)
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    • 2 cyclizes polyenes in a stepwise fashion that produces partially cyclized products. See for example:, H. Takao, A. Wakabayashi, K. Takahashi, H. Imagawa, T. Sugihara, M. Nishizawa, Tetrahedron Lett. 2004, 45, 1079-1082.
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    • For important contributions to dicationic pincer-platinum alkene activations, see
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    • Premature termination of a polyene cyclization can be viewed as an alkene terminated reaction.
    • Premature termination of a polyene cyclization can be viewed as an alkene terminated reaction.
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    • Allylsilanes, enolsilanes, enolethers, vinyl fluorides, and vinyl silanes have previously been used as relatively polarized alkene terminators, see references [1, 2, 8, and 16]
    • Allylsilanes, enolsilanes, enolethers, vinyl fluorides, and vinyl silanes have previously been used as relatively polarized alkene terminators, see references [1, 2, 8, and 16].
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    • II wherein a terminal carbenium ion was proposed. See for example
    • II wherein a terminal carbenium ion was proposed. See for example
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    • note
    • See the Supporting Information for X-ray data. CCDC c08276 (3), c08373 (9), x1007026 (11), c08380 (13), and c08394 (15) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
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    • 2-initiated cyclization of the terminal epoxy analogue of 8 gave both the tri- and tetrasubstituted alkenes, see reference [8]
    • 2-initiated cyclization of the terminal epoxy analogue of 8 gave both the tri- and tetrasubstituted alkenes, see reference [8].
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    • For a contrasting example see compound 30 in reference [8]
    • For a contrasting example see compound 30 in reference [8].
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    • MacSpartan 2008 calculations; energies were uncorrected
    • MacSpartan 2008 calculations; energies were uncorrected.
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    • For recent high-level computational studies of cation-olefin reactions and rearrangements in terpene biosynthesis, see:, and references therein.
    • For recent high-level computational studies of cation-olefin reactions and rearrangements in terpene biosynthesis, see:, D. J. Tantillo, Chem. Soc. Rev. 2010, 39, 2847-2854, and references therein.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.