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Volumn 53, Issue 4, 2014, Pages 1135-1139

Rhodium(I)-catalyzed cyclization of allenynes with a carbonyl group through unusual insertion of a C=O bond into a rhodacycle intermediate

Author keywords

alkynes; allenes; carbonyl compounds; cycloadditions; rhodium

Indexed keywords

ALKYNES; ALLENES; CYCLOADDITIONS; HYDRIDE ELIMINATION; REDUCTIVE ELIMINATION; SEVEN-MEMBERED RINGS; TRANSITION STATE; TRICYCLIC PRODUCTS;

EID: 84893230673     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201308824     Document Type: Article
Times cited : (31)

References (79)
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    • I-catalyzed [2+2+2] cycloaddition of allenynes with C=O bonds.
    • I-catalyzed [2+2+2] cycloaddition of allenynes with C=O bonds:, Y. Oonishi, Y. Kitano, Y. Sato, Tetrahedron 2013, 69, 7713.
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    • Oonishi, Y.1    Kitano, Y.2    Sato, Y.3
  • 57
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    • [5+2] cycloaddition of 3-acyloxy-1,4-enyne
    • Angew. Chem. Int. Ed. 2010, 49, 2206; [5+2] cycloaddition of 3-acyloxy-1,4-enyne
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2206
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    • I-catalyzed cyclization of allenyne through C-H bond activation
    • I-catalyzed cyclization of allenyne through C-H bond activation:, Y. Oonishi, Y. Kitano, Y. Sato, Angew. Chem. 2012, 124, 7158
    • (2012) Angew. Chem. , vol.124 , pp. 7158
    • Oonishi, Y.1    Kitano, Y.2    Sato, Y.3
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    • also see Ref. [12j].
    • Angew. Chem. Int. Ed. 2012, 51, 7052, and also see Ref. [12j].
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 7052
  • 77
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    • I-catalyzed cycloaddition. According to these previous methods, however, 8-oxabicyclo[3.2.1]octane skeleton having an oxygen-bridged structure cannot be constructed. Also, see.
    • I-catalyzed cycloaddition. According to these previous methods, however, 8-oxabicyclo[3.2.1]octane skeleton having an oxygen-bridged structure cannot be constructed. Also, see:, K. E. O. Ylijoki, J. M. Stryker, Chem. Rev. 2013, 113, 2244.
    • (2013) Chem. Rev. , vol.113 , pp. 2244
    • Ylijoki, K.E.O.1    Stryker, J.M.2
  • 78
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    • CCDC 963500 (7 j) and 963499 (6 p) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.