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Volumn 50, Issue 16, 2011, Pages 3784-3787

Discovery of stabilized bisiodonium salts as intermediates in the carbon-carbon bond formation of alkynes

Author keywords

Alkynes; Bridging ligands; Cyclization; Iodine; Spiro compounds

Indexed keywords

ALKYNES; ARYL ALKYNES; BRIDGING LIGANDS; C-C BOND FORMATION; CARBON-CARBON BOND FORMATION; CHEMICAL EQUATIONS; FACILE CONVERSION; FUNCTIONALIZED; HYPERVALENT IODINE COMPOUNDS; SECONDARY BONDING; SPIRO COMPOUNDS; SYNTHETIC UTILITY;

EID: 79953692993     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201007640     Document Type: Article
Times cited : (81)

References (45)
  • 16
    • 79953696605 scopus 로고    scopus 로고
    • CCDC 779156 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The via For more detailed crystallographic data, see the CIF
    • CCDC 779156 contains 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. For more detailed crystallographic data, see the CIF.
  • 20
    • 79953687472 scopus 로고    scopus 로고
    • note
    • We have confirmed that the concept is also applicable to other types of carbon-carbon and carbon-heteroatom bond-forming events. Details will be summarized in due course.
  • 21
    • 63849267472 scopus 로고    scopus 로고
    • For the utility of spirocyclic compounds, see the following reviews: a and references therein
    • For the utility of spirocyclic compounds, see the following reviews: a) S. Kotha, A. C. Deb, K. Lahiri, E. Manivannan, Synthesis 2009, 165, and references therein;
    • (2009) Synthesis , pp. 165
    • Kotha, S.1    Deb, A.C.2    Lahiri, K.3    Manivannan, E.4
  • 28
    • 79953714956 scopus 로고    scopus 로고
    • note
    • aryl-I bond.
  • 29
    • 27544441150 scopus 로고    scopus 로고
    • For the synthesis of spirocyclic compounds with the introduction of a nucleophile, see: a
    • For the synthesis of spirocyclic compounds with the introduction of a nucleophile, see: a) F. C. Pigge, J. J. Coniglio, N. P. Rath, Organometallics 2005, 24, 5424;
    • (2005) Organometallics , vol.24 , pp. 5424
    • Pigge, F.C.1    Coniglio, J.J.2    Rath, N.P.3
  • 31
    • 24644449080 scopus 로고    scopus 로고
    • Most established methods for the synthesis of functionalized spirocyclic compounds could accommodate the introduction of electrophiles into the structures; for recent studies, see: a
    • Most established methods for the synthesis of functionalized spirocyclic compounds could accommodate the introduction of electrophiles into the structures; for recent studies, see: a) X. Zhang, R. C. Larock, J. Am. Chem. Soc. 2005, 127, 12230;
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 12230
    • Zhang, X.1    Larock, R.C.2
  • 34
    • 79953725817 scopus 로고    scopus 로고
    • note
    • 2) could also be obtained from a series of aryl alkynes 3 in good yields.
  • 35
    • 0000491742 scopus 로고    scopus 로고
    • For the general utility of alkenyl iodonium salts, see: a
    • For the general utility of alkenyl iodonium salts, see: a) N. S. Pirkuliev, V. K. Brel, N. S. Zefirov, Russ. Chem. Rev. 2000, 69, 105;
    • (2000) Russ. Chem. Rev. , vol.69 , pp. 105
    • Pirkuliev, N.S.1    Brel, V.K.2    Zefirov, N.S.3
  • 36
    • 0038445018 scopus 로고    scopus 로고
    • Hypervalent Iodine Chemistry
    • Ed.: T. Wirth, Springer, Berlin
    • b) "Hypervalent Iodine Chemistry": M. Ochiai in Topics in Current Chemistry, Vol. 224 (Ed.: T. Wirth), Springer, Berlin, 2003, p. 5;
    • (2003) Topics in Current Chemistry , vol.224 , pp. 5
    • Ochiai, M.1
  • 39
    • 70449597257 scopus 로고    scopus 로고
    • see also Ref. [1]
    • Angew. Chem. Int. Ed. 2009, 48, 9052; see also Ref. [1].
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9052


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.