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Volumn 29, Issue 24, 2010, Pages 6632-6635

A unique functional group transformation of planar chiral diolefinic organonitrogen cycles utilizing PtCl2(2,4,6-trimethylpyridine) Complexes

Author keywords

[No Author keywords available]

Indexed keywords

FUNCTIONAL GROUP TRANSFORMATIONS; NMR AND X-RAY; STEREOSPECIFIC;

EID: 78650653089     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om1009704     Document Type: Article
Times cited : (11)

References (49)
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    • Details will be reported separately
    • Details will be reported separately.
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    • For a review on the electrophilic activation of alkenes by Pt(II), see
    • For a review on the electrophilic activation of alkenes by Pt(II), see: Chianese, A. R.; Lee, S. J.; Gagné, M. R. Angew. Chem., Int. Ed. 2007, 46, 4042-4059
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 4042-4059
    • Chianese, A.R.1    Lee, S.J.2    Gagné, M.R.3
  • 24
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    • 2 fragment than is ethylene
    • 2 fragment than is ethylene. Morokuma, K.; Borden, W. T. J. Am. Chem. Soc. 1991, 113, 1912-1914
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  • 33
    • 0032785772 scopus 로고    scopus 로고
    • 2(pybox- ip)[(-)-(E)-cyclooctene] (from 150.6 to 148.7 Hz); see: Similar changes for (±)- 4a, (±)- 4b, and their congeners will be measured and reported separately
    • 2(pybox- ip)[(-)-(E)-cyclooctene] (from 150.6 to 148.7 Hz); see: Nishiyama, H.; Naitoh, T.; Motoyama, Y.; Aoki, K. Chem. Eur. J. 1999, 3509-3513 Similar changes for (±)- 4a, (±)- 4b, and their congeners will be measured and reported separately.
    • (1999) Chem. Eur. J. , pp. 3509-3513
    • Nishiyama, H.1    Naitoh, T.2    Motoyama, Y.3    Aoki, K.4
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    • references therein
    • Tsipis, A. C. Organometallics 2008, 27, 3701-3713 and references therein.
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    • Tsipis, A.C.1
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    • 3 solution, despite the unsymmetrical structure of their olefinic units (see the Supporting Information)
    • 3 solution, despite the unsymmetrical structure of their olefinic units (see the Supporting Information).
  • 39
    • 0012879192 scopus 로고
    • As early as 1969, Orchin and co-workers reported (14a) that pyridinic ligands undergo more rapid ligand exchange with solvent molecules than olefinic ligands in this class of compounds, but the anomalous feature of 3 arising from 2,6-disubstitution at the pyridine nuclei has been documented later by a number of research groups (3b-3f) including themselves. (14b)
    • As early as 1969, Orchin and co-workers reported (14a) that pyridinic ligands undergo more rapid ligand exchange with solvent molecules than olefinic ligands in this class of compounds, but the anomalous feature of 3 arising from 2,6-disubstitution at the pyridine nuclei has been documented later by a number of research groups (3b-3f) including themselves. (14b) Kaplan, P. D.; Schmidt, P.; Brause, A.; Orchin, M. J. Am. Chem. Soc. 1969, 91, 85-88
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 85-88
    • Kaplan, P.D.1    Schmidt, P.2    Brause, A.3    Orchin, M.4
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    • The thermolysis of (±)- 4b in toluene at 80°C for 1.5 h resulted in its complete consumption to give a mixture, from which (±)- 6b was isolated in 54% yield
    • The thermolysis of (±)- 4b in toluene at 80°C for 1.5 h resulted in its complete consumption to give a mixture, from which (±)- 6b was isolated in 54% yield.
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    • 5, although similar reaction conditions have been very effective for the preparation of the series (±)- 1a - d
    • 5, although similar reaction conditions have been very effective for the preparation of the series (±)- 1a - d.
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    • 1H} NMR data for the coordinated olefinic parts of (±)- 4ax, (±)- 4bx, (±)- 4ay, and (±)- 5a are compiled in the Supporting Information
    • 1H} NMR data for the coordinated olefinic parts of (±)- 4ax, (±)- 4bx, (±)- 4ay, and (±)- 5a are compiled in the Supporting Information.
  • 49
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    • The solid-state structures of (±)- 4bx and (±)- 5a were also determined by X-ray diffraction. See the Supporting Information
    • The solid-state structures of (±)- 4bx and (±)- 5a were also determined by X-ray diffraction. See the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.