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Volumn 131, Issue 49, 2009, Pages 17836-17842

Remarkable product diversity in the "self-organized" reaction of deprotonated acetonitrile with chlorophosphines

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL SUBSTITUENT; CYCLOHEXYL; ELEMENTAL ANALYSIS; FUNCTIONALIZED; IN-SITU; NMR SPECTROSCOPY; OVERALL REACTIONS; PRODUCT DIVERSITY; SELF-ORGANIZED; THREE COMPONENT REACTIONS; TYPE STRUCTURES;

EID: 71749086324     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja905676a     Document Type: Article
Times cited : (8)

References (81)
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    • See for a comparison: (a)
    • See for a comparison: (a) Schmidpeter, A.; Zeiss, W. Angew. Chem. 1971, 11, 397-398.
    • (1971) Angew. Chem. , vol.11 , pp. 397-398
    • Schmidpeter, A.1    Zeiss, W.2
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    • 0007453818 scopus 로고
    • Zh. Obshch. Khim., 1993 63, 1767-1775.
    • (1993) Zh. Obshch. Khim. , vol.63 , pp. 1767-1775
  • 72
    • 71749121437 scopus 로고    scopus 로고
    • For organic reactions of R-metallated nitrile substrates see, for example: (a)
    • For organic reactions of R-metallated nitrile substrates see, for example: (a) Fleming, F. F.; Liu, W. Eur. J. Org. Chem. 2009, 69, 9-708.
    • (2009) Eur. J. Org. Chem. , vol.69 , pp. 9-708
    • Fleming, F.F.1    Liu, W.2
  • 76
    • 36248957093 scopus 로고    scopus 로고
    • For silyl acetonitriles, see: and references cited therein
    • For silyl acetonitriles, see: Krempner, C.; Martens, K.; Reinke, H. J. Organomet. Chem. 2007, 692, 5799-5803, and references cited therein.
    • (2007) J. Organomet. Chem. , vol.692 , pp. 5799-5803
    • Krempner, C.1    Martens, K.2    Reinke, H.3
  • 77
    • 84984178543 scopus 로고
    • For germyl acetonitriles, see: (a)
    • For germyl acetonitriles, see: (a) Wiberg, N.; Kim, C.-K. Chem. Ber. 1986, 119, 2966-2979.
    • (1986) Chem. Ber. , vol.119 , pp. 2966-2979
    • Wiberg, N.1    Kim, C.-K.2
  • 81
    • 71749099184 scopus 로고    scopus 로고
    • Due to a 33% impurity, the initial amount of the starting material was higher to achieve 1.0 equiv of chlorodimesitylphosphine
    • Due to a 33% impurity, the initial amount of the starting material was higher to achieve 1.0 equiv of chlorodimesitylphosphine.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.