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Volumn 133, Issue 20, 2011, Pages 7621-7623

Computationally designed and experimentally confirmed diastereoselective rhodium-catalyzed Pauson-Khand reaction at room temperature

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION BARRIERS; CHARGE POLARIZATION; COMPUTATIONAL ANALYSIS; DIASTEREOISOMERS; DIASTEREOSELECTIVE; DIASTEREOSELECTIVE REACTIONS; ELECTRON WITHDRAWING GROUP; EXPERIMENTAL STUDIES; PAUSON-KHAND REACTIONS; RHODIUM-CATALYZED; ROOM TEMPERATURE; TRANSITION STATE;

EID: 79957736107     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja107895g     Document Type: Article
Times cited : (38)

References (27)
  • 1
    • 33845435469 scopus 로고    scopus 로고
    • For recent reviews of transition metal-catalyzed higher-order carbocyclization reactions, see
    • For recent reviews of transition metal-catalyzed higher-order carbocyclization reactions, see: Aubert, C.; Fensterbank, L.; Gandon, V.; Malacria, M. Top. Organomet. Chem. 2006, 19, 259
    • (2006) Top. Organomet. Chem. , vol.19 , pp. 259
    • Aubert, C.1    Fensterbank, L.2    Gandon, V.3    Malacria, M.4
  • 3
    • 3342979429 scopus 로고    scopus 로고
    • For recent examples of DFT calculations on the understanding of rhodium-catalyzed [ m + n ] and [ m + n + o ] carbocyclization reactions, see the following. [(5+2)]
    • For recent examples of DFT calculations on the understanding of rhodium-catalyzed [ m + n ] and [ m + n + o ] carbocyclization reactions, see the following. [(5+2)]: Yu, Z.-X.; Wender, P. A.; Houk, K. N. J. Am. Chem. Soc. 2004, 126, 9154
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 9154
    • Yu, Z.-X.1    Wender, P.A.2    Houk, K.N.3
  • 8
    • 84890780346 scopus 로고    scopus 로고
    • For recent reviews of PK reactions, see: In;, Ed.; Wiley-VCH: Weinheim, Ch. 11, pp.
    • For recent reviews of PK reactions, see: Jeong, N. In Modern Rhodium-Catalyzed Organic Reactions; Evans, P. A., Ed.; Wiley-VCH: Weinheim, 2005, Ch. 11, pp 215.
    • (2005) Modern Rhodium-Catalyzed Organic Reactions , pp. 215
    • Jeong, N.1    Evans, P.A.2
  • 17
    • 9144236440 scopus 로고    scopus 로고
    • For the challenges associated with conducting room-temperature PK reactions, see
    • For the challenges associated with conducting room-temperature PK reactions, see: Schmid, T. M.; Consiglio, G. Chem. Commun. 2004, 2318
    • (2004) Chem. Commun. , pp. 2318
    • Schmid, T.M.1    Consiglio, G.2
  • 18
    • 84986513567 scopus 로고
    • We use the CHELP charges, as defined in
    • We use the CHELP charges, as defined in Breneman, C. M.; Wiberg, K. B. J. Comput. Chem. 1990, 11, 361
    • (1990) J. Comput. Chem. , vol.11 , pp. 361
    • Breneman, C.M.1    Wiberg, K.B.2
  • 19
    • 79957731679 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.
  • 23
    • 79957677367 scopus 로고    scopus 로고
    • The C4/C4′-positions are too close to the highly polarizable metal center to provide much information with regard to the electronic reorganization
    • The C4/C4′-positions are too close to the highly polarizable metal center to provide much information with regard to the electronic reorganization.
  • 24
    • 10044224654 scopus 로고    scopus 로고
    • For examples of metal-catalyzed [ m + n ] and [ m + n + o ] carbocyclizations with alkynyl halides, see the following. Ru [(2+2)]
    • For examples of metal-catalyzed [ m + n ] and [ m + n + o ] carbocyclizations with alkynyl halides, see the following. Ru [(2+2)]: Villenueve, K.; Riddell, N.; Jordan, R. W.; Tsui, G. C.; Tam, W. Org. Lett. 2004, 6, 4543
    • (2004) Org. Lett. , vol.6 , pp. 4543
    • Villenueve, K.1    Riddell, N.2    Jordan, R.W.3    Tsui, G.C.4    Tam, W.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.